CNGH0010 Specific Polynucleotides, Polypeptides, Antibodies, Compositions, Methods and Uses

ABSTRACT

Novel polypeptides (CNGH0010) and antibodies, including specified portions or variants, specific for at least one such CNGH0010 polypeptide, variant, or fragment thereof, as well as nucleic acids encoding such CNGH0010 polypeptides and antibodies, complementary nucleic acids, vectors, host cells, and methods of making and using thereof, are useful for therapeutic and diagnostic formulations, administration and devices. The aforesaid polypeptides can be used to generate human, primate, rodent, mammalian, chimeric, humanized and/or CDR-grafted anti-CNGH0010 antibodies. The CNGH0010 polypeptides and antibodies are used in modulating or treating at least one CNGH0010-related disease in a cell, tissue, organ, animal, or patient. Such diseases may include, but are not limited to, psoriasis, rheumatoid arthritis, emphysema, asthma, diabetes, autoimmune thyroiditis, inflammatory bowel diseases, including Crohn&#39;s disease and ulcerative colitis, different types of dermatitis including allergic dermatitis, contact dermatitis, actinic keratosis, wound healing, scar formation, various renal diseases, various respiratory diseases, various diseases of reproductive organs, such as endometriosis, melanoma, squamous cell carcinoma, ovarian cancer, breast cancer, lung cancer, colon cancer, prostate cancer, renal cell carcinoma, Grave&#39;s diseases and other inflammatory and hyperproliferative diseases.

CROSS-REFERENCED TO RELATED APPLICATION

The present application claims the benefit of priority of U.S. Provisional Application Ser. No. 60/777,740, filed 28 Feb. 2006, and is a continuation-in-part of U.S. application Ser. No. 10/835,904, filed 30 Apr. 2004, currently pending, which claims priority to U.S. Provisional Application Ser. No. 60/466,573, filed 30 Apr. 2003. The entire contents of the foregoing applications are incorporated herein in their entirety.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to CNGH0010 polypeptides, variants, and fragments thereof, and antibodies and anti-idiotype antibodies specific therefor, as well as nucleic acids encoding such CNGH0010 polypeptides, variants, fragments, antibodies, complementary nucleic acids, vectors, host cells, and methods of making and using thereof, including diagnostic and therapeutic formulations, administration and devices.

2. Background and Related Art

Psoriasis is a genetic, multifactoral, chronic inflammatory skin disease, with a prevalence of 2.6% in the U.S. population. The disease is characterized by pronounced hyperproliferation of keratinocytes, which results in rapid epidermal turnover and thickened, scaly, red plaques observed clinically. Other prominent histopathological features of the disease are alterations of cytokine production, fibroblast activation, vascular expansion, and leukocyte infiltration in the dermis and epidermis. Dysregulation in cytokine production from both activated cells in the dermis and the immune cells seems to play an important role in mediating the inflammatory events associated with psoriasis. To this end, a number of changes in gene and/or protein expression have been described previously in psoriasis and some of these genes and/or proteins have also been found to be associated with other inflammatory diseases. These include proinflammatory cytokines such as IL-1 and TNFα, adhesion molecules, such as intercellular adhesion molecule 1 (ICAM1) and vascular adhesion molecule 1 (VCAM1), chemokines, and defensins. Recently, gene expression microarray technology has been applied to profile gene expression patterns in normal versus psoriatic lesional skins on a more inclusive scale and has provided new insights into the pathogenesis of psoriasis.

cDNA microarray technology provides a format for the simultaneous measurement of the expression level of thousands of genes in a single hybridization assay. It is also amenable to an automated, high-throughput format. More importantly, microarray technology can be used to discover new genes, quantify and analyze gene expression and assign functionality to genes with unknown function. With the complete sequencing of the human genome, identification and cloning of new genes is now accomplished rapidly. However, the understanding of whether these genes encode new proteins and the further identification of the function of these new proteins have not advanced as rapidly. The impediment has become one of the main reasons for the use of high throughput cDNA microarray technology in a well-designed experimental setting to discover novel protein-encoding genes or genes with novel functions that may subsequently become potential therapeutic targets for a variety of human diseases.

Accordingly, there is a need to provide new polypeptides, polynucleotides, antibodies, or fragments thereof and uses thereof relevant to diseases and conditions, as well as improvements over known polypeptides, polynucleotides, antibodies or fragments thereof.

SUMMARY OF THE INVENTION

The present invention relates to an isolated CNGH0010 polypeptide having the sequence shown in one of SEQ ID NOS:3, 5, 7, 9, 11, and 41, variants, for example, those based on differential exon splicing as described in Table 2 below, and fragments thereof. Another aspect of the invention is an isolated polynucleotide comprising the sequence shown in one of SEQ ID NOS:2, 4, 6, 8, 10, and 40, variants (e.g., those based on differential exon splicing as described in Table 2 below) and fragments thereof, and complementary sequences. Another aspect of the invention is an isolated polynucleotide comprising a polynucleotide encoding the amino acid sequence shown in one of SEQ ID NOS:3, 5, 7, 9, 11, and 41, variants (e.g., those based on differential exon splicing as described in Table 2 below) and fragments thereof, and complementary sequences.

The invention also relates to isolated polypeptides having at least 70%, preferably, 75%, 80%, 90%, 95%, 99%, or 100% amino acid sequence identity to any of the amino acid sequences of SEQ ID NOS:3, 5, 7, 9, 11, and 41, variants, or fragments thereof, isolated polynucleotides having at least 70%, preferably, 75%, 80%, 90%, 95%, 99%, or 100% nucleic acid sequence identity to any of the polynucleotide sequences of SEQ ID NOS:2, 4, 6, 8, 10, and 40, variants, complementary sequences, or fragments thereof, and isolated polynucleotides having at least 70%, preferably, 75%, 80%, 90%, 95%, 99%, or 100% nucleic acid sequence identity to the polynucleotides encoding any of the amino acid sequences of SEQ ID NOS:3, 5, 7, 9, 11, and 41, and variants, complementary sequences, or fragments thereof.

The present invention also provides isolated nucleic acid molecules hybridizing to (a) a nucleic acid molecule encoding a polypeptide which has at least 70% amino acid sequence identity to an amino acid sequence of one of SEQ ID NOS:3, 5, 7, 9, 11, and 41, variants, and fragments thereof, or (b) a nucleic acid molecule having at least 70% sequence identity to any of the polynucleotide sequences of SEQ ID NOS:2, 4, 6, 8, 10, and 40, variants, and fragments thereof, and complementary nucleic acids. The present invention further provides recombinant vectors comprising the polypeptide encoding nucleic acid molecules, host cells containing such nucleic acids and/or recombinant vectors, as well as methods of making and/or using such nucleic acids, vectors and/or host cells.

In another aspect, the present invention relates to antibodies and antibody fragments capable of binding to (a) a polypeptide having at least 70% amino acid sequence identity to all or part of an amino acid sequence of one of SEQ ID NOS:3, 5, 7, 9, 11, and 41 or variants, or (b) a polypeptide encoded by a polynucleotide having at least 70% nucleic acid identity to all or part of any of the polynucleotide sequences of SEQ ID NOS:2, 4, 6, 8, 10, and 40 or variants. In addition, the invention comprises antibody compositions, formulations, devices, and transgenic mice and plants. The present invention also provides methods for generating and characterizing human, primate, rodent, mammalian, chimeric, single chain, humanized and/or CDR-grafted anti-CNGH0010 antibodies, immunoglobulins, cleavage products and other specified portions and variants thereof. The present invention further provides at least one CNGH0010 anti-idiotype antibody to at least one CNGH0010 antibody of the present invention.

The nucleic acid sequences encoding CNGH0010 polypeptides, or fragments thereof, can be operably linked to a nucleic acid sequence encoding a heterologous amino acid sequence to form a fusion protein. A further embodiment is a mimetibody which comprises at least a fragment of a CNGH0010 polypeptide fused to at least part of an immunoglobulin region. A preferred mimetibody comprises at least one CH₃ region directly linked with at least one CH₂ region directly linked with at least one hinge region or fragment thereof optionally directly linked with at least one partial V region, directly linked with an optional linker sequence, directly linked to at least a fragment of a CNGH0010 polypeptide, optionally, further directly linked with at least a portion of at least one variable antibody sequence. In a further preferred embodiment, the immunoglobulin is IgG1 or IgG4.

Another aspect of the invention provides recombinant expression vectors, comprising a CNGH0010 polynucleotide. In another embodiment, the invention provides isolated host cells, e.g., mammalian and non-mammalian cells, containing such a vector and/or a CNGH0010 polynucleotide. The invention also provides methods for producing a CNGH0010 polypeptide by culturing, in a suitable medium, a host cell of the invention containing a recombinant expression vector encoding a CNGH0010 polypeptide such that the polypeptide is produced.

The present invention also provides at least one method for expressing a CNGH0010 polypeptide, anti-CNGH0010 antibody, or CNGH0010 anti-idiotype antibody, in a host cell, comprising culturing a host cell as described herein under conditions wherein at least one such CNGH0010 polypeptide, anti-CNGH0010 antibody or CNGH0010 anti-idiotype antibody is expressed in detectable and/or recoverable amounts.

In yet another aspect, the present invention provides a fusion protein comprising a polypeptide which has at least 70%, preferably, 75%, 80%, 90%, 95%, 99%, or 100% amino acid sequence identity to an amino acid sequence of one of SEQ ID NOS:3, 5, 7, 9, 11, and 41, fused to a heterologous amino acid sequence.

The present invention also provides at least one composition comprising (a) an isolated CNGH0010 polynucleotide, polypeptide, polypeptide agonist or antagonist, antibody, and/or anti-idiotype antibody as described herein; and (b) a suitable carrier or diluent. The carrier or diluent can optionally be pharmaceutically acceptable, according to known carriers or diluents. The composition can optionally further comprise at least one further compound, protein or composition.

The present invention also relates to methods of treatment and/or diagnosis of CNGH0010 related diseases, such as but not limited to, psoriasis, rheumatoid arthritis, emphysema, asthma, diabetes, autoimmune thyroiditis, inflammatory bowel diseases, including Crohn's disease and ulcerative colitis, different types of dermatitis including allergic dermatitis, contact dermatitis, actinic keratosis, wound healing, scar formation, various renal diseases, various respiratory diseases, various diseases of reproductive organs, such as endometriosis, melanoma, squamous cell carcinoma, ovarian cancer, breast cancer, lung cancer, colon cancer, prostate cancer, renal cell carcinoma, Grave's diseases and other inflammatory and hyperproliferative diseases. In a preferred embodiment, the CNGH0010 related disease is an epithelial-related disease or condition such that the disease or condition impacts epithelial cells and related cells, including, without limitation, psoriasis, inflammatory bowel diseases including Crohn's disease and ulcerative colitis, different types of dermatitis (allergic dermatitis, contact dermatitis), Actinic keratosis, wound healing, scar formation, different renal diseases, different respiratory diseases, different diseases of reproductive organs such as endometriosis, melanoma, squamous cell carcinoma, ovarian cancer, breast cancer, lung cancer, colon cancer, prostate cancer, renal cell carcinoma, emphysema, Grave's disease, diabetes, pemphigus, bullous pemphigoid, Herpes, Linear IgA disease, drug eruption, epidermolysis bullosa, stomatitis, aphthous ulcer, peptic ulcers, gastric polyposis, chronic obstructive pulmonary diseases, bronchiectasis, cystic fibrosis, renal cystic disease, cystitis, and other inflammatory and hyperproliferative diseases. The methods utilize (1) an isolated polypeptide comprising at least one of the sequences selected from SEQ ID NOS:3, 5, 7, 9, 11, and 41, variants, derivatives, and fragments thereof, (2) an isolated polynucleotide comprising at least one of the sequences of SEQ ID NOS:2, 4, 6, 8, 10, and 40, variants, derivatives, and fragments thereof, and complementary sequences, (3) an isolated polypeptide encoded by a polynucleotide comprising at least one of the sequences of SEQ ID NOS:2, 4, 6, 8, 10, and 40, variants and fragments thereof, and (4) agonists and antagonists to such polypeptides and nucleotide to diagnose and/or treat inflammatory and hyperproliferative diseases and conditions. The present invention also provides methods of treatment and/or diagnosis of CNGH0010 related diseases utilizing a CNGH0010 agonist or antagonist, anti-CNGH0010 antibody and/or CNGH0010 anti-idiotype antibody.

The present invention further provides any invention described herein.

DESCRIPTION OF THE FIGURES

FIG. 1 shows the genomic structure of the CNGH0010 gene with exons being represented by vertical lines and the transcription start sites represented by curved arrows.

FIG. 2 shows relative transcript levels as determined by RT-PCR using RNA from A431 cells.

FIG. 3 shows predicted protein domains based on expression data and analysis of the amino acids coded by CNGH0010 transcripts.

FIG. 4 shows SDS-PAGE analysis of CNGH0010.2 expressed in HEK293 cells in reduced and non-reduced samples.

FIG. 5 shows the mass spectrum analysis of CNGH0010 (exons 1-13).

FIG. 6 shows the SEC-HPLC analysis of CNGH0010 (exons 1-13).

FIG. 7 shows the glycosylation analysis of CNGH0010 (exons 1-13).

FIGS. 8A and 8B show the vector maps of the plasmids used to generate the CNGH0010 riboprobes. FIG. 8A shows the exons 1 and 2 specific riboprobe; FIG. 8B shows the exons 18-23 specific riboprobe.

FIGS. 9A-F show the results of in situ hybridization of CNGH0010 in human tissue samples (breast FIG. 9A, small intestine FIG. 9B, skin FIG. 9C, prostate FIG. 9D, liver FIG. 9E, pancreas FIG. 9F).

DESCRIPTION OF THE INVENTION

As used herein, “CNGH0010 polypeptide(s) or protein(s),” or “polypeptide(s) or protein(s) of the invention” encompass isolated polypeptides comprising at least one of the sequences selected from SEQ ID NOS:3, 5, 7, 9, 11, and 41, variants, derivatives, and fragments thereof. “CNGH0010 nucleic acids, polynucleotide(s), or gene(s),” or “nucleic acids, polynucleotide(s), or gene(s) of the invention” refer to isolated polynucleotides comprising at least one of the sequences of SEQ ID NOS:2, 4, 6, 8, 10, and 40, variants, derivatives, and fragments thereof, and complementary sequences.

Splice variants of the CNGH0010 protein and nucleic acids encoding these variants have been identified in epithelial cell types through use of RACE, RT-PCR, and Northern blot techniques. The exons and untranslated regions of the genomic CNGH0010 DNA sequence (SEQ ID NO: 1) were identified (Table 1). As shown in Table 2, the CNGH0010 gene has multiple possible variants as a result of differential transcription initiation and termination sites, i.e., alternative splicing. The primary variants are labeled CNGH0010.1, CNGH0010.2, CNGH0010.3, CNGH0010.4, CNGH0010.5, and truncated CNGH0010.2 (represented by SEQ ID NOS:2, 4, 6, 8, 10, and 40 (nucleic acids) and 3, 5, 7, 9, 11, and 41 (amino acids), respectively). Additional variants of the invention are encompassed by different combinations of exons as seen in analysis of the genomic sequence and RT-PCR products. This is demonstrated in Table 2 as shown by the exons that may be added or deleted to the coding sequences.

RT-PCR analysis of CNGH0010 transcripts present in A431 cells indicate that the CNGH0010.1 transcripts are heterogeneous with regard to the presence or absence of at least exons 11 and 20, whereas the CNGH0010.2 transcripts have heterogeneity with regard to exon 9. Also, CNGH0010.4 transcripts are heterogeneous with regard to the presence or absence of exons 9, 10, 11, and 12.

The similarities of the CNGH0010 molecules to extracellular matrix molecules (collagens) and cytokines (adiponectin) suggest that they may participate in the regulation of cell-cell or cell-matrix interactions, or bind to or influence the binding of a cytokine to a receptor. Both types of activities would ultimately influence the proliferation, migration, and differentiation status of cells and tissues. Therefore, proteins and polynucleotides of the invention represent ideal targets for therapeutic intervention using monoclonal antibodies, synthetic polypeptides, small molecule drugs, or other natural or synthetic drugs.

Accordingly, the present invention provides novel amino acid and nucleic acid sequences identified as the CNGH0010 protein and gene. The sequences comprise an isolated polypeptide comprising a polypeptide having the sequence shown in one of SEQ ID NOS:3, 5, 7, 9, 11, and 41 or variants thereof; an isolated polynucleotide comprising a polynucleotide having the sequence shown in one of SEQ ID NOS:2, 4, 6, 8, 10, and 40 or a complementary sequence; an isolated polynucleotide comprising a polynucleotide encoding the amino acid sequence shown in one of SEQ ID NOS:3, 5, 7, 9, 11, and 41 or a complementary sequence; isolated polypeptides comprising a polypeptide having at least 70% amino acid sequence identity to any of the amino acid sequences of SEQ ID NOS:3, 5, 7, 9, 11, and 41 or variants thereof; isolated polynucleotides having at least 70% nucleic acid sequence identity to any of the polynucleotide sequences of SEQ ID NOS:2, 4, 6, 8, 10, and 40, complementary sequences, or variants thereof; isolated polynucleotides having at least 70% nucleic acid sequence identity to the polynucleotides encoding any of the amino acid sequences of SEQ ID NOS:3, 5, 7, 9, 11, and 41, complementary sequences, or variants thereof; and isolated nucleic acid molecules hybridizing to a nucleic acid molecule encoding a polypeptide which has at least 70% amino acid sequence identity to an amino acid sequence of one of SEQ ID NOS:3, 5, 7, 9, 11, and 41, a nucleic acid molecule having at least 70% sequence identity to any of the polynucleotide sequences of SEQ ID NOS:2, 4, 6, 8, 10, and 40, or complementary nucleic acids; and fragments of these polypeptide and polynucleotide sequences.

As used herein, “identity,” as known in the art, is a relationship between two or more polypeptide sequences or two or more polynucleotide sequences, as determined by comparing the sequences. In the art, “identity” also means the degree of sequence relatedness between polypeptide or polynucleotide sequences, as determined by the match between strings of such sequences. “Identity” and “similarity” can be readily calculated by known methods, including, but not limited to, those described in (Computational Molecular Biology, Lesk, A. M., ed., Oxford University Press, New York, 1988; Biocomputing:Informatics and Genome Projects, Smith, D. W., ed., Academic Press, New York, 1993; Computer Analysis of Sequence Data, Part I, Griffin, A. M., and Griffin, H. G., eds., Humana Press, New Jersey, 1994; Sequence Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; and Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press, New York, 1991; and Carillo, H., and Lipman, D., Siam J. Applied Math., 48:1073 (1988). In addition, values for percentage identity can be obtained from amino acid and nucleotide sequence alignments generated using the default settings for the AlignX component of Vector NTI Suite 8.0 (Informax, Frederick, Md.).

Preferred methods to determine identity are designed to give the largest match between the sequences tested. Methods to determine identity and similarity are codified in publicly available computer programs. Preferred computer program methods to determine identity and similarity between two sequences include, but are not limited to, the GCG program package (Devereux, J., et al., Nucleic Acids Research 12(1): 387 (1984)), BLASTP, BLASTN, and FASTA (Atschul, S. F. et al., J. Molec. Biol. 215:403-410 (1990). The BLAST X program is publicly available from NCBI and other sources (BLAST Manual, Altschul, S., et al., NCBINLM NIH Bethesda, Md. 20894: Altschul, S., et al., J. Mol. Biol. 215:403-410 (1990). The well-known Smith Waterman algorithm may also be used to determine identity.

Preferred parameters for polypeptide sequence comparison include the following:

(1) Algorithm: Needleman and Wunsch, J. Mol. Biol. 48:443-453 (1970) Comparison matrix: BLOSSUM62 from Hentikoff and Hentikoff, Proc. Natl. Acad. Sci, USA. 89:10915-10919 (1992)

Gap Penalty: 12 Gap Length Penalty: 4

A program useful with these parameters is publicly available as the “gap” program from Genetics Computer Group, Madison Wis. The aforementioned parameters are the default parameters for polypeptide comparisons (along with no penalty for end gaps).

Preferred parameters for polynucleotide comparison include the following:

(1) Algorithm: Needleman and Wunsch, J. Mol. Biol. 48:443-453 (1970) Comparison matrix: matches=+10, mismatch=0

Gap Penalty: 50 Gap Length Penalty: 3

Available as: The “gap” program from Genetics Computer Group, Madison Wis. These are the default parameters for nucleic acid comparisons.

By way of example, a polynucleotide sequence of the present invention may be identical to the sequence of SEQ ID NO:2, that is be 100% identical, or it may include up to a certain integer number of nucleotide alterations as compared to the reference sequence. Such alterations are selected from the group consisting of at least one nucleotide deletion, substitution, including transition and transversion, or insertion, and wherein the alterations may occur at the 5′ or 3′ terminal positions of the reference nucleotide sequence or anywhere between those terminal positions, interspersed either individually among the nucleotides in the reference sequence or in one or more contiguous groups within the reference sequence. The number of nucleotide alterations is determined by multiplying the total number of nucleotides in SEQ ID NO:2 by the numerical percent of the respective percent identity (divided by 100) and subtracting that product from the total number of nucleotides in SEQ ID NO:2, or:

n.sub.n·ltorsim·x.sub.n−(x.sub.n.y),

wherein n.sub.n is the number of nucleotide alterations, x.sub.n is the total number of nucleotides in SEQ ID NO:2, and y is, for instance, 0.70 for 70%, 0.80 for 80%, 0.85 for 85%, 0.90 for 90%, 0.95 for 95%, etc., and wherein any non-integer product of x.sub.n and y is rounded down to the nearest integer prior to subtracting from x.sub.n.

Alterations of a polynucleotide sequence encoding the polypeptide of SEQ ID NO:3 may create nonsense, missense or frameshift mutations in this coding sequence and thereby alter the polypeptide encoded by the polynucleotide following such alterations. Similarly, a polypeptide sequence of the present invention may be identical to the reference sequence of SEQ ID NO:3, that is be 100% identical, or it may include up to a certain integer number of amino acid alterations as compared to the reference sequence such that the percentage identity is less than 100%. Such alterations are selected from the group consisting of at least one amino acid deletion, substitution, including conservative and non-conservative substitutions, or insertions, and wherein the alterations may occur at the amino- or carboxy-terminal positions of the reference polypeptide sequence or anywhere between those terminal positions, interspersed either individually among the amino acids in the reference sequence or in one or more contiguous groups within the reference sequence. The number of amino acid alterations for a given % identity is determined by multiplying the total number of amino acids in SEQ ID NO:3 by the numerical percent of the respective percent identity (divided by 100) and then subtracting that product from the total number of amino acids in SEQ ID NO:3, or:

n.sub.a·ltorsim·x.sub.a−(x.sub.a·y),

wherein n.sub.a is the number of amino acid alterations, x.sub.a is the total number of amino acids in SEQ ID NO:3, and y is, for instance, 0.70 for 70%, 0.80 for 80%, 0.85 for 85% etc., and wherein any non-integer produce of x.sub.a and y is rounded down to the nearest integer prior to subtracting it from x.sub.a.

As used herein, a “fragment” is a variant polypeptide having an amino acid sequence that is entirely the same as part but not all of any amino acid sequence of any polypeptide of the invention or a variant polynucleotide having a nucleic acid sequence that is entirely the same as part but not all of any nucleic acid sequence of any polynucleotide of the invention. Fragments can include, e.g., truncation polypeptides having a portion of an amino acid sequence as shown in the amino acid sequences of SEQ ID NOS:3, 5, 7, 9, 11, or 41 or of variants thereof, such as a continuous series of residues that include a heterologous amino- and/or carboxy-terminal amino acid sequence. Degradation forms of the polypeptides of the invention produced by or in a host cell are also included. Other exemplary fragments are characterized by structural or functional attributes, such as fragments that comprise alpha-helix or alpha-helix forming regions, beta-sheet or beta-sheet forming regions, turn or turn-forming regions, coil or coil-forming regions, hydrophilic regions, hydrophobic regions, alpha-amphipathic regions, beta-amphipathic regions, flexible regions, surface-forming regions, substrate binding regions, extracellular regions and high antigenic index regions.

Further exemplary fragments include an isolated polypeptide comprising an amino acid sequence having at least 15, 20, 30, 40, 50 or 100 contiguous amino acids from the amino acid sequence set forth in SEQ ID NOS:3, 5, 7, 9, 11 or 41 and variants, or an isolated polypeptide comprising an amino acid sequence having at least 15, 20, 30, 40, 50 or 100 contiguous amino acids truncated or deleted from the amino acid sequence set forth in amino acid sequence shown in SEQ ID NOS:3, 5, 7, 9, 11, or 41 and variants. Fragments also include isolated polynucleotides having similar sizes and characteristics.

The polypeptides and derivatives of the invention are useful as agents to inhibit the binding of the CNGH0010 polypeptide to its ligand and reduce or block subsequent signal transduction. The polypeptides and polypeptide constructs can be used as immunogens or as binding partners useful for generating, selecting, and characterizing human, primate, rodent, mammalian, chimeric, single chain, humanized and/or CDR-grafted anti-CNGH0010 antibodies, immunoglobulins, cleavage products and other specified portions and variants thereof. In addition, the antibody amino acid sequences, and encoding nucleic acid molecules comprising at least one polynucleotide encoding at least one anti-CNGH0010 antibody or anti-idiotype antibody can be determined by methods well-known in the art and as described herein.

At least one human CNGH0010 polypeptide sequence as described herein is antigenic and offers a method for the generation of anti-CNGH0010 antibodies. The polypeptides described herein comprise a new class of CNGH0010 antigens that contain critical epitopes for diagnostic and therapeutic CNGH0010 antibodies. The polypeptides can be synthesized as described herein based on the amino acid sequence of the human CNGH0010 polypeptide sequences of the invention.

The CNGH0010 polypeptide or anti-CNGH0010 antibody can be incorporated into a method or composition for administering a therapeutically or prophylactically effective amount to modulate or treat at least one CNGH0010-related condition in a cell, tissue, organ, animal or patient and/or, prior to, subsequent to, or during a related condition, as known in the art and/or as described herein. The CNGH0010 polypeptide or anti-CNGH0010 antibody can be incorporated into a method or composition for diagnosing at least one CNGH0010-related condition in a cell, tissue, organ, animal or patient and/or, prior to, subsequent to, or during a related condition, as known in the art and/or as described herein.

The CNGH0010 polypeptide or anti-CNGH0010 antibody can be incorporated into a method for diagnosing or treating a CNGH0010-related condition in a cell, tissue, organ or animal, comprising contacting or administering a composition comprising an effective amount of at least one isolated CNGH0010 polypeptide or anti-CNGH0010 antibody composition of the invention with, or to, the cell, tissue, organ or animal. The method can optionally further comprise using an effective amount of 0.001-50 mg/kilogram of the polypeptide or antibody. The method can optionally further comprise treating the CNGH0010-related condition with the polypeptide or antibody by administering the polypeptide or antibody by at least one mode selected from parenteral, subcutaneous, intramuscular, intravenous, intrarticular, intrabronchial, intraabdominal, intracapsular, intracartilaginous, intracavitary, intracelial, intracerebellar, intracerebroventricular, intracolic, intracervical, intragastric, intrahepatic, intramyocardial, intraosteal, intrapelvic, intrapericardiac, intraperitoneal, intrapleural, intraprostatic, intrapulmonary, intrarectal, intrarenal, intraretinal, intraspinal, intrasynovial, intrathoracic, intrauterine, intravesical, bolus, vaginal, rectal, buccal, sublingual, intranasal, and transdermal.

The present invention provides for novel proteins and polypeptides from CNGH0010's receptor binding region that can be used to generate anti-CNGH0010 antibodies and fragments thereof. First, the methods of identifying, isolating, and creating the novel polypeptides are discussed below. Then, the generation of antibodies, applications, formulations, and therapeutic treatments are presented.

All publications cited herein are entirely incorporated herein by reference, whether or not specifically designated accordingly, as they show the state of the art at the time of the present invention and/or to provide description and enablement of the present invention. Publications refer to any scientific or patent publications, or any other information available in any media format, including all recorded, electronic or printed formats. The following references are entirely incorporated herein by reference: Ausubel, et al., ed., Current Protocols in Molecular Biology, John Wiley & Sons, Inc., NY, N.Y. (1987-2001); Sambrook, et al., Molecular Cloning: A Laboratory Manual, 2nd Edition, Cold Spring Harbor, N.Y. (1989); Harlow and Lane, antibodies, a Laboratory Manual, Cold Spring Harbor, N.Y. (1989); Colligan, et al., eds., Current Protocols in Immunology, John Wiley & Sons, Inc., NY (1994-2001); Colligan et al., Current Protocols in Protein Science, John Wiley & Sons, NY, N.Y., (1997-2001).

A human CNGH0010 polypeptide of the present invention includes those of SEQ ID NOS:3, 5, 7, 9, 11, and 41 and their variants, including, without limitation, alternative splice variants, and can include one or more amino acid substitutions, deletions or additions, either from natural mutations or human manipulation, as specified herein. Such mutations or substitutions can include muteins, whose mutations can be significant enough to alter the properties of the polypeptide without altering the biological activity of the polypeptide to inhibit the binding of human CNGH0010 to its ligand. Included within the invention are CNGH0010 polypeptides having amino acid sequences in addition to those of SEQ ID NOS:3, 5, 7, 9, 11, and 41 and their variants.

Of course, the number of amino acid substitutions a skilled artisan would make depends on many factors, including those described above. Generally speaking, the number of amino acid substitutions, insertions or deletions for any given CNGH0010 polypeptide, fragment or variant will not be more than 1-5, or any range or value therein, as specified herein.

Amino acids in a CNGH0010 polypeptide of the present invention that are essential for function can be identified by methods known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (e.g., Ausubel, supra, Chapters 8, 15; Cunningham and Wells, Science 244:1081-1085 (1989)). The latter procedure introduces single alanine mutations at every residue in the molecule. The resulting mutant molecules are then tested for biological activity, such as, but not limited to, at least one CNGH0010 neutralizing activity.

Synthesis of CNGH0010 Polypeptides

Polypeptides having the amino acid sequences set forth and described above, may be synthesized using standard Boc or FMOC chemistry. The resulting polypeptides can be injected as is, cross-linked, or conjugated to a carrier molecule. To facilitate conjugation to carriers, an N-terminal N-acetyl-cysteine or C-terminal amides can be formed and the C-terminal amino acid can be amidated. A variety of linking groups may be interspaced between the polypeptide and the carrier molecule to allow for proper conformational folding and presentation of the antigenic polypeptide.

It is envisioned that the CNGH0010 polypeptides of this invention may also be produced by cell lines derived from bacteria, yeast, insect, or mammal. Recombinant expression cassettes comprising the nucleic acids encoding the novel polypeptides can be introduced into at least one host cell. Vectors containing the CNGH0010 nucleic acid sequence and necessary promoter elements may be used to express CNGH0010 polypeptides. Nucleic acid sequences encoding a CNGH0010 polypeptide in conjunction with a signal peptide may be included to facilitate secretion and purification of desired polypeptides. Those of ordinary skill in the art are knowledgeable in the numerous expression systems available for expression of a nucleic acid encoding a polypeptide of the present invention. Cell-free translation systems can also be employed to produce such polypeptides using RNAs derived from the DNA constructs of the invention.

Nucleic Acid Molecules

Nucleic acid sequences encoding human CNGH0010 polypeptides of the present invention may be obtained by cloning, for example, by RT-PCR amplification of RNA samples. Alternatively, the DNA encoding CNGH0010 polypeptides may be obtained by DNA synthesis or from any cDNA library prepared from tissues believed to possess the CNGH0010 mRNA or from a genomic DNA library. The nucleic acid sequences can be cloned by PCR amplification or by traditional methods of DNA hybridization and expression cloning.

Using the information provided herein (methods described herein or as known in the art), such as the nucleotide sequences encoding at least 70-100% of the contiguous amino acids of at least one of SEQ ID NOS:3, 5, 7, 9, 11, and 41 or specified fragments, variants or consensus sequences thereof, or a vector comprising at least one of these sequences, a nucleic acid molecule of the present invention encoding at least one CNGH0010 polypeptide or anti-CNGH0010 antibody can be obtained.

Nucleic acid molecules of the present invention can be in the form of RNA, such as mRNA, hnRNA, or any other form, or in the form of DNA, including, but not limited to, cDNA and genomic DNA obtained by cloning or produced synthetically, or any combinations thereof. The DNA can be triple-stranded, double-stranded or single-stranded, or any combination thereof. Any portion of at least one strand of the DNA or RNA can be the coding strand, also known as the sense strand, or it can be the non-coding strand, also referred to as the anti-sense strand.

As indicated herein, nucleic acid molecules of the present invention which comprise a nucleic acid encoding a CNGH0010 polypeptide or anti-CNGH0010 antibody can include, but are not limited to, those encoding the amino acid sequence of a polypeptide or antibody fragment, by itself, the coding sequence for the entire polypeptide or antibody or a portion thereof, the coding sequence for a polypeptide or antibody, fragment or portion, as well as additional sequences, such as the coding sequence of at least one signal leader or fusion peptide, with or without the aforementioned additional coding sequences, such as at least one intron, together with additional, non-coding sequences, including but not limited to, non-coding 5′ and 3′ sequences, such as the transcribed, non-translated sequences that play a role in transcription, mRNA processing, including splicing and polyadenylation signals (for example, ribosome binding and stability of mRNA); and an additional coding sequence that codes for additional amino acids, such as those that provide additional functionalities. Thus, the sequence encoding a polypeptide or antibody can be fused to a marker sequence, such as a sequence encoding a peptide that facilitates purification of the fused antibody comprising an antibody fragment or portion thereof.

Construction of Nucleic Acids and Expression and Purification of Polypeptides

The isolated nucleic acids of the present invention can be made using (a) recombinant methods, (b) synthetic techniques, (c) purification techniques, or combinations thereof, as well-known in the art.

The nucleic acids can conveniently comprise sequences in addition to a polynucleotide of the present invention. For example, a multi-cloning site comprising one or more endonuclease restriction sites can be inserted into the nucleic acid to aid in isolation of the polynucleotide. Also, translatable sequences can be inserted to aid in the isolation of the translated polynucleotide of the present invention. For example, a hexa-histidine marker sequence provides a convenient means to purify the proteins of the present invention. The nucleic acid of the present invention—excluding the coding sequence—is optionally a vector, adapter, or linker for cloning and/or expression of a polynucleotide of the present invention.

Additional sequences can be added to such cloning and/or expression sequences to optimize their function in cloning and/or expression, to aid in isolation of the polynucleotide, or to improve the introduction of the polynucleotide into a cell. Use of cloning vectors, expression vectors, adapters, and linkers is well known in the art. (See, e.g., Ausubel, supra; or Sambrook, supra)

A great variety of expression systems can be used to produce the polypeptides of the invention. Such systems include chromosomal-, episomal- and virus-derived vectors, such as vectors derived from bacterial plasmids, bacteriophage, transposons, yeast episomes, insertion elements, yeast chromosomal elements, baculoviruses, papova viruses, such as SV40, vaccinia viruses, adenoviruses, fowl pox viruses, pseudorabies viruses, picronaviruses and retroviruses and vectors derived from combinations thereof, such as cosmids and phagemids. The expression system constructs may contain control regions that regulate or cause expression. Generally, any system or vector suitable to maintain or propagate polynucleotides and/or to express polypeptides in a host may be used for expression. An appropriate DNA sequence may be inserted into the expression system by any of a variety of techniques well known to those skilled in the art, such as, e.g., those set forth in Sambrook et al, supra.

In eukaryotic expression systems, polypeptides of the invention can be secreted into the lumen of the endoplasmic reticulum or extracellular environment by inclusion of appropriate secretion signals, such as a signal peptide or leader sequence.

Polypeptides of the invention can be recovered and purified from recombinant cell cultures by well-known methods, including ammonium sulfate or ethanol precipitation, acid extraction, high-performance liquid chromatography, anion or cation exchange chromatography, phosphocellulose chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxyapatite chromatography and lectin chromatography. Well-known techniques for refolding protein may be employed to regenerate an active conformation when the protein is denatured during isolation and/or purification.

In an alternate method of obtaining the nucleic acid of the invention, encoding the CNGH0010 polypeptides, a cDNA or genomic library can be screened using a probe based upon the sequence of a polynucleotide of the present invention, such as those disclosed herein. Probes can be used to hybridize with genomic DNA or cDNA sequences to isolate homologous genes in the same or different organisms. Those of skill in the art will appreciate that various degrees of stringency of hybridization can be employed in the assay; and either the hybridization or the wash medium can be stringent. As the conditions for hybridization become more stringent, there must be a greater degree of complementarity between the probe and the target for duplex formation to occur. The degree of stringency can be controlled by one or more of temperature, ionic strength, pH and the presence of a partially denaturing solvent, such as formamide.

For example, the stringency of hybridization is conveniently varied by changing the polarity of the reactant solution through, for example, manipulation of the concentration of formamide within the range of 0% to 50%. The degree of complementarity (sequence identity) required for detectable binding will vary in accordance with the stringency of the hybridization medium and/or wash medium. The degree of complementarity will optimally be 100%, or 80-100%, or any range or value therein. However, it should be understood that minor sequence variations in the probes and primers can be compensated for by reducing the stringency of the hybridization and/or wash medium. An example of stringent hybridization conditions includes overnight incubation at 42° C. in a solution comprising: 50% formamide, 5×SSC (150 mM NaCl, 15 mM trisodium citrate), 50 mM sodium phosphate (pH 7.6), 5×Denhardt's solution, 10% dextran sulfate, and 20 microgram/ml denatured, sheared salmon sperm DNA; followed by washing the filters in 0.1×SSC at about 65° C.

Methods of amplification of RNA or DNA are well known in the art and can be used according to the present invention without undue experimentation, based on the teaching and guidance presented herein. Known methods of DNA or RNA amplification include, but are not limited to, polymerase chain reaction (PCR) and related amplification processes (see, e.g., U.S. Pat. Nos. 4,683,195, 4,683,202, 4,800,159, 4,965,188, to Mullis, et al.; 4,795,699 and 4,921,794 to Tabor, et al; 5,142,033 to Innis; 5,122,464 to Wilson, et al.; 5,091,310 to Innis; 5,066,584 to Gyllensten, et al; 4,889,818 to Gelfand, et al; 4,994,370 to Silver, et al; 4,766,067 to Biswas; 4,656,134 to Ringold) and RNA mediated amplification that uses anti-sense RNA to the target sequence as a template for double-stranded DNA synthesis (U.S. Pat. No. 5,130,238 to Malek, et al, with the tradename NASBA), the entire contents of which references are incorporated herein by reference. (See, e.g., Ausubel, supra; or Sambrook, supra.)

For instance, polymerase chain reaction (PCR) technology can be used to amplify the sequences of polynucleotides of the present invention and related genes directly from genomic DNA or cDNA libraries. PCR and other in vitro amplification methods can also be useful, for example, to clone nucleic acid sequences that code for proteins to be expressed, to make nucleic acids to use as probes for detecting the presence of the desired mRNA in samples, for nucleic acid sequencing, or for other purposes. Examples of techniques sufficient to direct persons of skill through in vitro amplification methods are found in Berger, supra, Sambrook, supra, and Ausubel, supra, as well as Mullis, et al., U.S. Pat. No. 4,683,202 (1987); and Innis, et al., PCR Protocols A Guide to Methods and Applications, Eds., Academic Press Inc., San Diego, Calif. (1990). Commercially available kits for genomic PCR amplification are known in the art. See, e.g., Advantage-GC Genomic PCR Kit (Clontech). Additionally, e.g., the T4 gene 32 protein (Boehringer Mannheim) can be used to improve yield of long PCR products.

The isolated nucleic acids of the present invention can also be prepared by direct chemical synthesis by known methods (see, e.g., Ausubel, et al., supra). Chemical synthesis generally produces a single-stranded oligonucleotide, which can be converted into double-stranded DNA by hybridization with a complementary sequence, or by polymerization with a DNA polymerase using the single strand as a template. One of skill in the art will recognize that while chemical synthesis of DNA can be limited to sequences of about 100 or more bases, longer sequences can be obtained by the ligation of shorter sequences.

Polynucleotides Selectively Hybridizing to a Polynucleotide as Described

As described above, the present invention provides isolated nucleic acids that hybridize under selective hybridization conditions to a polynucleotide disclosed herein. Thus, the polynucleotides of this embodiment can be used for isolating, detecting, and/or quantifying nucleic acids comprising such polynucleotides. For example, polynucleotides of the present invention can be used to identify, isolate, or amplify partial or full-length clones in a deposited library. In some embodiments, the polynucleotides are genomic or cDNA sequences isolated, or otherwise complementary to, a cDNA from a human or mammalian nucleic acid library.

Preferably, the cDNA library comprises at least 80% full-length sequences, preferably, at least 85% or 90% full-length sequences, and, more preferably, at least 95% full-length sequences. The cDNA libraries can be normalized to increase the representation of rare sequences. Low or moderate stringency hybridization conditions are typically, but not exclusively, employed with sequences having a reduced sequence identity relative to complementary sequences. Moderate and high stringency conditions can optionally be employed for sequences of greater identity. Low stringency conditions allow selective hybridization of sequences having about 70% sequence identity and can be employed to identify orthologous or paralogous sequences.

Optionally, polynucleotides of this invention will encode at least a portion of a protein or an antibody encoded by the polynucleotides described herein. The polynucleotides of this invention embrace nucleic acid sequences that can be employed for selective hybridization to a polynucleotide encoding a protein or an antibody of the present invention. See, e.g., Ausubel, supra; Colligan, supra, each entirely incorporated herein by reference.

Use of CNGH0010 Polypeptides and Polynucleotides

The polynucleotides and polypeptides of the invention are also useful for assaying a medium for the presence of a substance that modulates CNGH0010 protein function by affecting the binding of a CNGH0010 analog protein to cellular binding partners, such as the CNGH0010 receptor. Examples of modulators include polypeptides or small organic molecules.

Polypeptides of the invention may also be used to identify lead compounds for drug development. The structure of the polypeptides described herein can be readily determined by a number of methods such as NMR and X-ray crystallography. A comparison of the structures of polypeptides similar in sequence, but differing in the biological activities that they elicit in target molecules can provide information about the structure-activity relationship of the target. Information obtained from the examination of structure-activity relationships can be used to design either modified polypeptides, or other small molecules or lead compounds which can be tested for predicted properties as related to the target molecule. The activity of the lead compounds can be evaluated using assays similar to those described herein.

Information about structure-activity relationships may also be obtained from co-crystallization studies. In these studies, a polypeptide with a desired activity is crystallized in association with a target molecule, and the X-ray structure of the complex is determined. The structure can then be compared to the structure of the target molecule in its native state, and information from such a comparison may be used to design compounds expected to possess desired activities.

The invention also contemplates methods for identifying novel compounds that bind to the polypeptides of the invention thereby affecting a CNGH0010-signaling pathway. Protein-protein interactions may be identified using conventional methods such as co-immunoprecipitation, crosslinking and co-purification through gradients or chromatographic columns. Methods may also be employed that result in the simultaneous identification of genes which encode proteins interacting with a molecule. These methods include probing expression libraries with labeled molecules. Additionally, x-ray crystallographic studies may be used as a means of evaluating interactions with substances and molecules.

It will be appreciated that fusion proteins and recombinant proteins may be used in the above described methods. The reagents suitable for applying the methods of the invention to evaluate substances and compounds that affect or modulate a CNGH0010 signaling pathway may be packaged into convenient kits providing the necessary materials packaged into suitable containers. The kits may also include suitable supports useful in performing the methods of the invention.

Mature CNGH0010 or its analogs can be used to modulate, i.e., increase or decrease, eukaryotic cell activity and/or number, such as proliferation and activation. Moreover, mature CNGH0010 or its analogs can be used to regulate cell differentiation and migration. Since CNGH0010 can be secreted, mature CNGH0010 or its analogs can also be used to treat various kinds of immune-mediated inflammatory diseases that are dependent on cell proliferation, differentiation, and migration, such as but not limited to, psoriasis, rheumatoid arthritis, emphysema, asthma, diabetes, autoimmune thyroiditis, inflammatory bowel diseases, including Crohn's disease and ulcerative colitis, different types of dermatitis including allergic dermatitis, contact dermatitis, actinic keratosis, wound healing, scar formation, various renal diseases, various respiratory diseases, various diseases of reproductive organs, such as endometriosis, melanoma, squamous cell carcinoma, ovarian cancer, breast cancer, lung cancer, colon cancer, prostate cancer, renal cell carcinoma, Grave's diseases and other inflammatory and hyperproliferative diseases. In addition, mature CNGH0010 or its analogs can be used to enhance immune responses to an infectious disease. Mature CNGH0010 or its analogs can be used alone or in combination with an antigen as an adjuvant to treat or prevent various infectious, hyperprolifeative and inflammatory diseases.

The mode of administration for therapeutic use of the polypeptides of the invention may be any suitable route that delivers the agent to the host, such as parenteral, subcutaneous, intramuscular, intravenous, intrarticular, intrabronchial, intraabdominal, intracapsular, intracartilaginous, intracavitary, intracelial, intracerebellar, intracerebroventricular, intracolic, intracervical, intragastric, intrahepatic, intramyocardial, intraosteal, intrapelvic, intrapericardiac, intraperitoneal, intrapleural, intraprostatic, intrapulmonary, intrarectal, intrarenal, intraretinal, intraspinal, intrasynovial, intrathoracic, intrauterine, intravesical, intralesional, bolus, vaginal, rectal, buccal, sublingual, intranasal, or transdermal.

Polypeptides of the invention may be prepared as pharmaceutical compositions containing an effective amount of the binding agent as an active ingredient in a pharmaceutically acceptable carrier. An aqueous suspension or solution containing the binding agent, preferably buffered at physiological pH, in a form ready for injection is preferred. The compositions for parenteral administration will commonly comprise a solution of the binding agent of the invention or a cocktail thereof dissolved in a pharmaceutically acceptable carrier, preferably, an aqueous carrier. A variety of aqueous carriers may be employed, e.g., 0.4% saline, 0.3% glycine and the like. These solutions are sterile and generally free of particulate matter. These solutions may be sterilized by conventional, well known sterilization techniques (e.g., filtration). The compositions may contain pharmaceutically acceptable auxiliary substances as required to approximate physiological conditions, such as pH adjusting and buffering agents, etc. The concentration of the polypeptides of the invention in such pharmaceutical formulations can vary widely, i.e., from less than about 0.5%, usually at or at least about 1% to as much as 15 or 20% by weight, and will be selected primarily based on fluid volumes, viscosities, etc., according to the particular mode of administration selected.

Thus, a pharmaceutical composition of the invention for intramuscular injection could be prepared to contain 1 mL sterile buffered water, and between about 1 ng to about 100 mg, e.g., about 50 ng to about 30 mg or more, preferably, about 5 mg to about 25 mg, of a polypeptide of the invention. Similarly, a pharmaceutical composition of the invention for intravenous infusion could be made up to contain about 250 ml of sterile Ringer's solution, and about 1 mg to about 30 mg and preferably 5 mg to about 25 mg of a polypeptide of the invention. Actual methods for preparing parenterally administrable compositions are well known or will be apparent to those skilled in the art and are described in more detail in, for example, Remington, the Science and Practice of Pharmacy, 19th ed., Mack Publishing Company, Easton, Pa. (1995).

The polypeptides of the invention, when in a pharmaceutical preparation, can be present in unit dose forms. The appropriate therapeutically effective dose can be determined readily by those of skill in the art. A determined dose may, if necessary, be repeated at appropriate time intervals that are selected as appropriate by a physician during the treatment period.

The polypeptides of the invention can be lyophilized for storage and reconstituted in a suitable carrier prior to use. This technique has been shown to be effective with conventional protein preparations and lyophilization and reconstitution techniques known in the art can be employed.

If a polypeptide of the present invention is to be expressed for use in screening assays, it is generally preferred that the polypeptide be produced at the surface of the cell. In this event, the cells may be harvested prior to use in the screening assay. If the polypeptide is secreted into the medium, the medium can be recovered in order to recover and purify the polypeptide. If produced intracellularly, the cell must first be lysed before the polypeptide is recovered.

This invention also relates to the use of polynucleotides of the present invention as diagnostic reagents. Detection of a mutated form of the gene characterized by the polynucleotide of SEQ ID NO:2 which is associated with a dysfunction will provide a diagnostic tool that can add to, or define, a diagnosis of a disease, or susceptibility to a disease, which results from under-expression, over-expression or altered expression of the gene. Individuals carrying mutations in the gene may be detected at the DNA level by a variety of techniques.

Nucleic acids for diagnosis may be obtained from a subject's cells, such as from blood, urine, saliva, tissue biopsy or autopsy material. The genomic DNA may be used directly for detection or may be amplified enzymatically by using PCR or other amplification techniques prior to analysis. RNA or cDNA may also be used in similar fashion. Deletions and insertions can be detected by a change in size of the amplified product in comparison to the normal genotype. Point mutations can be identified by hybridizing amplified DNA to labeled CNGH0010 nucleotide sequences. Perfectly matched sequences can be distinguished from mismatched duplexes by RNase digestion or by differences in melting temperatures. DNA sequence differences may also be detected by alterations in electrophoretic mobility of DNA fragments in gels, with or without denaturing agents, or by direct DNA sequencing (e.g., Myers et al., Science (1985) 230:1242). Sequence changes at specific locations may also be revealed by nuclease protection assays, such as RNase and S1 protection or the chemical cleavage method (see Cotton et al., Proc Natl Acad Sci USA (1985) 85:4397-4401). In another embodiment, an array of oligonucleotides probes comprising CNGH0010 nucleotide sequences or fragments thereof can be constructed to conduct efficient screening of e.g., genetic mutations. Array technology methods are well known and have general applicability and can be used to address a variety of questions in molecular genetics, including gene expression, genetic linkage, and genetic variability (see for example: M. Chee et al., Science, Vol 274, pp 610-613 (1996)).

The diagnostic assays offer a process for diagnosing or determining a susceptibility to the relevant diseases through detection of mutation in the CNGH0010 gene by the methods described. In addition, such diseases may be diagnosed by methods comprising determining from a sample derived from a subject an abnormally decreased or increased level of polypeptide or mRNA. Decreased or increased expression can be measured at the RNA level using any of the methods well known in the art for the quantitation of polynucleotides, such as, for example, nucleic acid amplification, for instance, PCR, RT-PCR, RNase protection, Northern blotting and other hybridization methods. Assay techniques that can be used to determine levels of a protein, such as a polypeptide of the present invention, in a sample derived from a host are well-known to those of skill in the art. Such assay methods include radioimmunoassays, competitive-binding assays, Western Blot analysis and ELISA assays.

Thus in another aspect, the present invention relates to a diagnostic kit which comprises:

(a) a polynucleotide of the present invention, preferably, one of the nucleotide sequences of SEQ ID NOS:2, 4, 6, 8, 10, and 40 and variants, polynucleotides with at least 70% identity to any of SEQ ID NOS:2, 4, 6, 8, 10, and 40 or variants, or a fragment thereof, (b) a nucleotide sequence complementary to that of (a); (c) a polypeptide of the present invention, preferably, one of the polypeptides of SEQ ID NOS:3, 5, 7, 9, 11, and 41 and variants, polypeptides with at least 70% identity to any of SEQ ID NOS:3, 5, 7, 9, 11, and 41 and variants, or a fragment thereof, or (d) an antibody to a polypeptide of the present invention, variants, and fragments thereof, preferably, to one of the polypeptides of SEQ ID NOS:3, 5, 7, 9, 11, and 41 and variants.

It will be appreciated that in any such kit, components (a), (b), (c), or (d) from above may comprise a substantial component. Such a kit will be of use in diagnosing a disease or susceptibility to a disease, such as but not limited to, psoriasis, rheumatoid arthritis, emphysema, asthma, diabetes, autoimmune thyroiditis, inflammatory bowel diseases including Crohn's disease and ulcerative colitis, various types of dermatitis including allergic dermatitis, contact dermatitis, actinic keratosis, wound healing, scar formation, various renal diseases, various respiratory diseases, various diseases of reproductive organs, such as endometriosis, melanoma, squamous cell carcinoma, ovarian cancer, breast cancer, lung cancer, colon cancer, prostate cancer, renal cell carcinoma, Grave's diseases and other inflammatory and hyperproliferative diseases.

The nucleotide sequences of the present invention are also valuable for chromosome identification. Each genomic sequence is specifically targeted to, and can hybridize with, a particular location on an individual human chromosome. The mapping of relevant sequences to chromosomes according to the present invention may be useful in correlating those sequences with gene-associated diseases and conditions. Once a sequence has been mapped to a precise chromosomal location, the physical position of the sequence on the chromosome can be correlated with genetic map data. Such data are found in, for example, V. McKusick, Mendelian Inheritance in Man (available on-line through Johns Hopkins University Welch Medical Library). The relationship between genes and diseases that have been mapped to the same chromosomal region can then be identified through linkage analysis (i.e., coinheritance of physically adjacent genes).

The differences in the cDNA or genomic sequence between affected and unaffected individuals can also be determined. If a mutation is observed in some or all of the affected individuals but not in any normal individuals, then the mutation is likely to be the causative agent of the disease. The polynucleotides, polypeptides and antibodies to the polypeptides of the present invention may also be used to configure screening methods for detecting the effect of added compounds on the production of mRNA and polypeptide in cells. For example, an ELISA assay may be constructed for measuring secreted or cell-associated levels of polypeptide using monoclonal and polyclonal antibodies by standard methods known in the art. This can be used to discover agents that may inhibit or enhance the production of polypeptide (also called antagonist or agonist, respectively) from suitably manipulated cells or tissues.

The polypeptide may be used to identify membrane bound or soluble receptors, if any, through standard receptor binding techniques known in the art. These include, but are not limited to, ligand binding and crosslinking assays in which the polypeptide is labeled with a radioactive isotope (for instance, ¹²⁵I), chemically modified (for instance, biotinylated), or fused to a peptide sequence suitable for detection or purification, and incubated with a source of the putative receptor (cells, cell membranes, cell supernatants, tissue extracts, bodily fluids). Other methods include biophysical techniques, such as surface plasmon resonance and spectroscopy. These screening methods may also be used to identify agonists and antagonists of the polypeptide that compete with the binding of the polypeptide to its receptors, if any. Standard methods for conducting these assays are well understood in the art.

Examples of potential polypeptide antagonists include antibodies or, in some cases, oligonucleotides or proteins which are closely related to the ligands, substrates, receptors, enzymes, etc., of the polypeptide. For example, a fragment of the ligands, substrates, receptors, enzymes, etc.; or small molecules may bind to the polypeptide of the present invention but may not elicit a response, i.e., to the activity of the polypeptide.

Thus in another aspect, the present invention relates to a screening kit for identifying agonists, antagonists, ligands, receptors, substrates, enzymes, etc. for polypeptides of the present invention; or compounds which decrease or enhance the production of such polypeptides, which comprises:

(a) a polypeptide of the present invention; (b) a recombinant cell expressing a polypeptide of the present invention; (c) a cell membrane expressing a polypeptide of the present invention; or (d) antibody to a polypeptide of the present invention, which polypeptide is preferably one of SEQ ID NOS:3, 5, 7, 9, 11, and 41 or splice variants.

It will be appreciated that in any such kit, components (a), (b), (c), or (d) may comprise a substantial component.

It will be readily appreciated by the skilled artisan that a polypeptide of the present invention may also be used in a method for the structure-based design of an agonist, antagonist or inhibitor of the polypeptide, by:

(a) determining in the first instance the three-dimensional structure of the polypeptide; (b) deducing the three-dimensional structure for the likely reactive or binding site(s) of an agonist, antagonist or inhibitor; (c) synthesizing candidate compounds that are predicted to bind to or react with the deduced binding or reactive site; and (d) testing whether the candidate compounds are indeed agonists, antagonists or inhibitors.

It will be further appreciated that this will normally be an interactive process.

Polypeptides used in treatment can also be generated endogenously in the subject, in treatment modalities often referred to as “gene therapy” as described above. Thus, for example, cells from a subject may be engineered with a polynucleotide, such as a DNA or RNA, to encode a polypeptide ex vivo, and for example, by the use of retroviral plasmid vector. The cells are then introduced into the subject.

Anti-CNGH0010 Antibodies

An antibody of the invention binds at least one specified epitope specific to a CNGH0010 protein, subunit, fragment, portion of the invention, or any combination thereof. The epitope can comprise an antibody binding region that comprises at least one portion of the amino acid sequence of SEQ ID NOS:3, 5, 7, 9, 11, and 41 or its variants (e.g., splice variants described below), which epitope is preferably comprised of at least 1-5 amino acids of the sequences. The antibody can include or be derived from any mammal, such as, but not limited to, a human, a mouse, a rabbit, a rat, a rodent, a primate, or any combination thereof, and the like.

An anti-CNGH0010 antibody, as described herein, has at least one activity, such as, but not limited to neutralizing CNGH0010-dependent receptor phosphorylation, receptor internalization, cell adhesion, migration and invasion, and induction of signaling molecules or adaptation of cell markers. An anti-CNGH0010 antibody can thus be screened for a corresponding activity according to known methods, such as but not limited to, at least one biological activity of human CNGH0010. The antibody can be used to measure or affect a cell, tissue, organ or animal (including mammals and humans), to diagnose, monitor, modulate, treat, alleviate, help prevent the incidence of, or reduce the symptoms of, at least one CNGH0010-related disease or condition, selected from, but not limited to, at least one of an immune disorder or disease, a cardiovascular disorder or disease, an infectious, malignant, and/or neurologic disorder or disease, or other known or specified CNGH0010-related condition.

Definition & Characterization of an Anti-CNGH0010 Antibody

As used herein, an “anti-CNGH0010 antibody,” “anti-CNGH0010 antibody portion,” or “anti-CNGH0010 antibody fragment” and/or “anti-CNGH0010 antibody variant” and the like include any protein or polypeptide containing molecule that comprises at least a portion of an immunoglobulin molecule, such as but not limited to, at least one complementarity determining region (CDR) of a heavy or light chain or a ligand binding portion thereof, a heavy chain or light chain variable region, a heavy chain or light chain constant region, a framework region, or any portion thereof, or at least one portion of a CNGH0010 receptor or binding protein derived from a CNGH0010 protein or polypeptide of the invention, which can be incorporated into an antibody of the present invention. Such antibody optionally further affects a specific ligand, such as but not limited to, where such antibody modulates, decreases, increases, antagonizes, angonizes, mitigates, alleviates, blocks, inhibits, abrogates and/or interferes with at least one CNGH0010 activity or binding, or with CNGH0010 ligand activity or binding, in vitro, in situ and/or in vivo. As a non-limiting example, a suitable anti-CNGH0010 antibody, specified portion or variant of the present invention can bind at least one CNGH0010 protein or polypeptide of the invention, or specified portions, variants or domains thereof. A suitable anti-CNGH0010 antibody, specified portion, or variant can also optionally affect at least one of CNGH0010 activity or function, such as but not limited to, RNA, DNA or protein synthesis, CNGH0010 release, CNGH0010 receptor signaling, CNGH0010 activity, CNGH0010 production and/or synthesis.

The term “antibody” is further intended to encompass antibodies, digestion fragments, specified portions and variants thereof, including antibody mimetics or portions of antibodies that mimic the structure and/or function of an antibody or specified fragment or portion thereof, including single chain antibodies and fragments thereof. Functional fragments include antigen-binding fragments that bind to a mammalian CNGH0010. For example, antibody fragments capable of binding to CNGH0010 or portions thereof, including, but not limited to, Fab (e.g., by papain digestion), Fab′ (e.g., by pepsin digestion and partial reduction) and F(ab′)2 (e.g., by pepsin digestion), facb (e.g., by plasmin digestion), pFc′ (e.g., by pepsin or plasmin digestion), Fd (e.g., by pepsin digestion, partial reduction and reaggregation), Fv or scFv (e.g., by molecular biology techniques) fragments, are encompassed by the invention (see, e.g., Colligan, Immunology, supra).

Such fragments can be produced by enzymatic cleavage, synthetic or recombinant techniques, as known in the art and/or as described herein. Antibodies can also be produced in a variety of truncated forms using antibody genes in which one or more stop codons have been introduced upstream of the natural stop site. For example, a combination gene encoding a F(ab′)2 heavy chain portion can be designed to include DNA sequences encoding the CH₁ domain and/or hinge region of the heavy chain. The various portions of antibodies can be joined together chemically by conventional techniques, or can be prepared as a contiguous protein using genetic engineering techniques.

As used herein, the term “human antibody” refers to an antibody in which substantially every part of the protein (e.g., CDR, framework, CL, CH domains (e.g., CH₁, CH₂, CH₃), hinge, (VL, VH)) is substantially non-immunogenic in humans, with only minor sequence changes or variations. Similarly, antibodies designated primate (monkey, baboon, chimpanzee, etc.), rodent (mouse, rat, rabbit, guinea pig, hamster, and the like) and other mammals designate such species, sub-genus, genus, sub-family, family specific antibodies. Further, chimeric antibodies of the invention can include any combination of the above. Such changes or variations optionally and preferably retain or reduce the immunogenicity in humans or other species relative to non-modified antibodies. Thus, a human antibody is distinct from a chimeric or humanized antibody. It is pointed out that a human antibody can be produced by a non-human animal or prokaryotic or eukaryotic cell that is capable of expressing functionally rearranged human immunoglobulin (e.g., heavy chain and/or light chain) genes. Further, when a human antibody is a single chain antibody, it can comprise a linker peptide that is not found in native human antibodies. For example, a Fv can comprise a linker peptide, such as 2 to about 8 glycine or other amino acid residues, which connects the variable region of the heavy chain and the variable region of the light chain. Such linker peptides are considered to be of human origin.

The isolated antibodies of the present invention comprise any isolated or prepared antibody prepared as described herein. Preferably, the human antibody or antigen-binding fragment binds human CNGH0010 and, thereby, partially or substantially neutralizes at least one biological activity of the protein. An antibody, or specified portion or variant thereof, that partially or preferably substantially neutralizes at least one biological activity of at least one CNGH0010 protein or fragment can bind the protein or fragment and thereby inhibit activities mediated through the binding of CNGH0010 to the CNGH0010 receptor or through other CNGH0010-dependent or mediated mechanisms. As used herein, the term “neutralizing antibody” refers to an antibody that can inhibit a CNGH0010-dependent activity by about 20-120%, preferably by at least about 10, 20, 30, 40, 50, 55, 60, 65, 70, 75, 80, 85, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100% or more depending on the assay. The capacity of an anti-CNGH0010 antibody to inhibit a CNGH0010-dependent activity is preferably assessed by at least one suitable CNGH0010 protein or receptor assay, as described herein and/or as known in the art. A human antibody of the invention can be of any class (IgG, IgA, IgM, IgE, IgD, etc.) or isotype and can comprise a kappa or lambda light chain. In one embodiment, the human antibody comprises an IgG heavy chain or defined fragment, for example, at least one of isotypes, IgG1, IgG2, IgG3 or IgG4. Antibodies of this type can be prepared by employing a transgenic mouse or other transgenic non-human mammal comprising at least one human light chain (e.g., IgG, IgA and IgM (e.g., γ1, γ2, γ3, γ4) transgenes as described herein and/or as known in the art. In another embodiment, the anti-human CNGH0010 human antibody comprises an IgG1 heavy chain and an IgG1 light chain.

At least one antibody of the invention binds at least one specified epitope specific to at least one CNGH0010 protein, subunit, fragment, portion or any combination thereof, as described herein. The at least one epitope can comprise at least one antibody binding region that comprises at least one portion of the protein sequences corresponding to the peptide sequences from the receptor binding region of human CNGH0010, as described herein, which epitope is preferably comprised of at least one extracellular, soluble, hydrophilic, external or cytoplasmic portion of the protein.

Generally, the human antibody or antigen-binding fragment of the present invention will comprise an antigen-binding region that comprises at least one human complementarity determining region (CDR1, CDR2 and CDR3) or variant of at least one heavy chain variable region and at least one human complementarity determining region (CDR1, CDR2 and CDR3) or variant of at least one light chain variable region.

Bispecific, heterospecific, heteroconjugate or similar antibodies can also be used that are monoclonal, preferably, human or humanized, antibodies that have binding specificities for at least two different antigens. In the present case, one of the binding specificities is for at least one CNGH0010 protein of the invention, the other one is for any other antigen. Methods for making bispecific antibodies are known in the art. Traditionally, the recombinant production of bispecific antibodies is based on the co-expression of two immunoglobulin heavy chain-light chain pairs, where the two heavy chains have different specificities (Milstein and Cuello, Nature 305:537 (1983)). Because of the random assortment of immunoglobulin heavy and light chains, these hybridomas (quadromas) produce a potential mixture of 10 different antibody molecules, of which only one has the correct bispecific structure. The purification of the correct molecule, which is usually done by affinity chromatography steps, is rather cumbersome, and the product yields are low. Similar procedures are disclosed, e.g., in WO 93/08829, U.S. Pat. Nos. 6,210,668, 6,193,967, 6,132,992, 6,106,833, 6,060,285, 6,037,453, 6,010,902, 5,989,530, 5,959,084, 5,959,083, 5,932,448, 5,833,985, 5,821,333, 5807706, 5643759, 5601819, 5582996, 5496549, and 4676980, WO 91/00360, WO 92/00373, EP 03089, Traunecker et al., EMBO J. 10:3655 (1991), and Suresh et al., Methods in Enzymology 121:210 (1986), each entirely incorporated herein by reference.

Anti-CNGH0010 antibodies useful in the methods and compositions of the present invention can optionally be characterized by high affinity binding to CNGH0010 and, optionally and preferably, having low toxicity. In particular, an antibody, specified fragment or variant of the invention, where the individual components, such as the variable region, constant region and framework, individually and/or collectively, optionally and preferably, possess low immunogenicity, is useful in the present invention. The antibodies that can be used in the invention are optionally characterized by their ability to treat patients for extended periods with measurable alleviation of symptoms and low and/or acceptable toxicity. Low or acceptable immunogenicity and/or high affinity, as well as other suitable properties, can contribute to the therapeutic results achieved. “Low immunogenicity” is defined herein as raising significant HAHA, HACA or HAMA responses in less than about 75%, or preferably less than about 50% of the patients treated and/or raising low titres in the patient treated (less than about 300, preferably, less than about 100 measured with a double antigen enzyme immunoassay) (Elliott et al., Lancet 344:1125-1127 (1994), entirely incorporated herein by reference).

Application of the anti-CNGH0010 antibody can comprise administering an effective amount of a composition or a pharmaceutical composition comprising at least one anti-CNGH0010 antibody to a cell, tissue, organ, animal, or patient in need of such modulation, treatment, alleviation, prevention, or reduction in symptoms, effects or mechanisms. The effective amount can comprise an amount of about 0.001 to 500 mg/kg per single (e.g., bolus), multiple or continuous administration, or to achieve a serum concentration of 0.01-5000 μg/ml serum concentration per single, multiple, or continuous administration, or any effective range or value therein, as done and determined using known methods, as described herein or known in the relevant arts.

As those of skill will appreciate, the present invention includes at least one biologically active antibody of the present invention. Biologically active antibodies have a specific activity at least 20%, 30%, or 40%, and, preferably, at least 50%, 60%, or 70%, and, most preferably, at least 80%, 90%, or 95%-100% of that of the native (non-synthetic), endogenous or related and known antibody. Methods of assaying and quantifying measures of enzymatic activity and substrate specificity are well known to those of skill in the art.

In another aspect, the invention relates to human antibodies and antigen-binding fragments, as described herein, which are modified by the covalent attachment of an organic moiety. Such modification can produce an antibody or antigen-binding fragment with improved pharmacokinetic properties (e.g., increased in vivo serum half-life). The organic moiety can be a linear or branched hydrophilic polymeric group, fatty acid group, or fatty acid ester group. Lipid molecules such as a disteroylphosphatidyl ethanolamine moiety, either alone or covalently bonded to a hydrophilic polymer, are useful. In particular embodiments, the hydrophilic polymeric group can have a molecular weight of about 800 to about 120,000 Daltons and can be a polyalkane glycol (e.g., polyethylene glycol (PEG), polypropylene glycol (PPG)), carbohydrate polymer, amino acid polymer or polyvinyl pyrolidone, and the fatty acid or fatty acid ester group can comprise from about eight to about forty carbon atoms.

The modified antibodies and antigen-binding fragments of the invention can comprise one or more organic moieties that are covalently bonded, directly or indirectly, to the antibody. Each organic moiety that is bonded to an antibody or antigen-binding fragment of the invention can independently be a hydrophilic polymeric group, a fatty acid group or a fatty acid ester group. As used herein, the term “fatty acid” encompasses mono-carboxylic acids and di-carboxylic acids. A “hydrophilic polymeric group,” as the term is used herein, refers to an organic polymer that is more soluble in water than in octane. For example, polylysine is more soluble in water than in octane. Thus, an antibody modified by the covalent attachment of polylysine is encompassed by the invention. Hydrophilic polymers suitable for modifying antibodies of the invention can be linear or branched and include, for example, polyalkane glycols (e.g., PEG, monomethoxy-polyethylene glycol (mPEG), PPG and the like), carbohydrates (e.g., dextran, cellulose, oligosaccharides, polysaccharides and the like), polymers of hydrophilic amino acids (e.g., polylysine, polyarginine, polyaspartate and the like), polyalkane oxides (e.g., polyethylene oxide, polypropylene oxide and the like) and polyvinyl pyrolidone. Preferably, the hydrophilic polymer that modifies the antibody of the invention has a molecular weight of about 800 to about 150,000 Daltons as a separate molecular entity. For example, PEG₅₀₀₀ and PEG_(20,000), wherein the subscript is the average molecular weight of the polymer in Daltons, can be used. The hydrophilic polymeric group can be substituted with one to about six alkyl, fatty acid or fatty acid ester groups. Hydrophilic polymers that are substituted with a fatty acid or fatty acid ester group can be prepared by employing suitable methods. For example, a polymer comprising an amine group can be coupled to a carboxylate of the fatty acid or fatty acid ester, and an activated carboxylate (e.g., activated with N,N-carbonyl diimidazole) on a fatty acid or fatty acid ester can be coupled to a hydroxyl group on a polymer.

Fatty acids and fatty acid esters suitable for modifying antibodies of the invention can be saturated or can contain one or more units of unsaturation. Fatty acids that are suitable for modifying antibodies of the invention include, for example, n-dodecanoate (C12, laurate), n-tetradecanoate (C14, myristate), n-octadecanoate (C18, stearate), n-eicosanoate (C20, arachidate), n-docosanoate (C22, behenate), n-triacontanoate (C30), n-tetracontanoate (C40), cis-Δ9-octadecanoate (C18, oleate), all cis-Δ5,8,11,14-eicosatetraenoate (C20, arachidonate), octanedioic acid, tetradecanedioic acid, octadecanedioic acid, docosanedioic acid, and the like. Suitable fatty acid esters include mono-esters of dicarboxylic acids that comprise a linear or branched lower alkyl group. The lower alkyl group can comprise from one to about twelve, preferably, one to about six, carbon atoms.

The modified human antibodies and antigen-binding fragments can be prepared using suitable methods, such as by reaction with one or more modifying agents. A “modifying agent” as the term is used herein, refers to a suitable organic group (e.g., hydrophilic polymer, a fatty acid, a fatty acid ester) that comprises an activating group. An “activating group” is a chemical moiety or functional group that can, under appropriate conditions, react with a second chemical group thereby forming a covalent bond between the modifying agent and the second chemical group. For example, amine-reactive activating groups include electrophilic groups such as tosylate, mesylate, halo (chloro, bromo, fluoro, iodo), N-hydroxysuccinimidyl esters (HS), and the like. Activating groups that can react with thiols include, for example, maleimide, iodoacetyl, acrylolyl, pyridyl disulfides, 5-thiol-2-nitrobenzoic acid thiol (TNB-thiol), and the like. An aldehyde functional group can be coupled to amine- or hydrazide-containing molecules, and an azide group can react with a trivalent phosphorous group to form phosphoramidate or phosphorimide linkages. Suitable methods to introduce activating groups into molecules are known in the art (see for example, Hermanson, G. T., Bioconjugate Techniques, Academic Press: San Diego, Calif. (1996)). An activating group can be bonded directly to the organic group (e.g., hydrophilic polymer, fatty acid, fatty acid ester), or through a linker moiety, for example, a divalent C1-C12 group wherein one or more carbon atoms can be replaced by a heteroatom such as oxygen, nitrogen or sulfur. Suitable linker moieties include, for example, tetraethylene glycol, —(CH₂)₃—, —NH—(CH₂)₆—NH—, —(CH₂)₂—NH— and —CH₂—O—CH₂—CH₂—O—CH₂—CH₂—O—CH—NH—. Modifying agents that comprise a linker moiety can be produced, for example, by reacting a mono-Boc-alkyldiamine (e.g., mono-Boc-ethylenediamine, mono-Boc-diaminohexane) with a fatty acid in the presence of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) to form an amide bond between the free amine and the fatty acid carboxylate. The Boc protecting group can be removed from the product by treatment with trifluoroacetic acid (TFA) to expose a primary amine that can be coupled to another carboxylate as described, or can be reacted with maleic anhydride and the resulting product cyclized to produce an activated maleimido derivative of the fatty acid. (See, for example, Thompson, et al., WO 92/16221, the entire teachings of which are incorporated herein by reference.)

The modified antibodies of the invention can be produced by reacting a human antibody or antigen-binding fragment with a modifying agent. For example, the organic moieties can be bonded to the antibody in a non-site specific manner by employing an amine-reactive modifying agent, for example, a NHS ester of PEG. Modified human antibodies or antigen-binding fragments can also be prepared by reducing disulfide bonds (e.g., intra-chain disulfide bonds) of an antibody or antigen-binding fragment. The reduced antibody or antigen-binding fragment can then be reacted with a thiol-reactive modifying agent to produce the modified antibody of the invention. Modified human antibodies and antigen-binding fragments comprising an organic moiety that is bonded to specific sites of an antibody of the present invention can be prepared using suitable methods, such as reverse proteolysis (Fisch et al., Bioconjugate Chem., 3:147-153 (1992); Werlen et al., Bioconjugate Chem., 5:411-417 (1994); Kumaran et al., Protein Sci. 6(10):2233-2241 (1997); Itoh et al., Bioorg. Chem., 24(1): 59-68 (1996); Capellas et al., Biotechnol. Bioeng., 56(4):456-463 (1997)), and the methods described in Hermanson, G. T., Bioconjugate Techniques, Academic Press: San Diego, Calif. (1996).

Generation of Monoclonal Antibodies

Monoclonal antibodies of this invention may be raised by traditional immunization and hybridoma technology. After immunization of mice with human CNGH0010 antigenic compositions comprising the polypeptides of the invention, spleen cells or lymphocytes from lymph node tissue from immunized animals are recovered and immortalized by fusion with myeloma cells or by Epstein-Barr (EB)-virus transformation. Monoclonal antibodies are obtained by screening for clones expressing the desired antibody. While mice are frequently employed as the test model, it is contemplated that any mammalian subject, including human subjects or antibody-producing cells, can be manipulated according to the processes of this invention to serve as the basis for production of mammalian, including human and hybrid cell lines. Techniques for cloning recombinant DNA of antibody molecule directly from an antibody-expressing B cell are within the scope of this invention. Such B cells can be isolated by the fluorescence activated cell sorter.

While routinely, mouse monoclonal antibodies are generated, the invention is not so limited. For therapeutic applications, human or humanized antibodies are desired. Such antibodies can be obtained by using human hybridomas or by generating humanized antibodies. Humanized antibodies can be developed by replacing the specific segments of a non-human antibody with corresponding segments of a human antibody gene. This process retains most or all of CDR regions of the light and heavy chain variable regions of parental antibody and largely replaces the framework regions with human sequences [EP Patent No. 184187; EP Patent No. 171496; EP Patent No. 173494 and WO Patent No. 86/01533]. Human monoclonal antibodies are also generated in transgenic mice that contain genes or gene segments encoding human antibodies in their genome [U.S. Pat. No. 6,162,963; WO Patent No. 93/12227; U.S. Pat. No. 5,877,5397; U.S. Pat. No. 5,874,299; U.S. Pat. No. 5,814,318; U.S. Pat. No. 5,789,650; U.S. Pat. No. 5,770,429; U.S. Pat. No. 5,661,016; U.S. Pat. No. 5,625,126; U.S. Pat. No. 5,569,825; U.S. Pat. No. 5,545,806; and WO Patent No. 91/10741].

Human monoclonal antibodies are also obtained from recombinant antibody libraries, generated in vitro or in vivo, using phage display, ribosome display, or related screening or selection techniques. Examples of procedures for generating antibody libraries, primarily of human origin, are disclosed by A. Knappik and others [65] [U.S. Pat. No. 6,291,158; U.S. Pat. No. 6,291,159; U.S. Pat. No. 6,291,160 and U.S. Pat. No. 6,291,161]. Examples of methods for selections of human antibodies to specific antigen targets from such libraries are disclosed by B. Krebs and others [66] [U.S. Pat. No. 5,955,341; U.S. Pat. No. 5,759,817; U.S. Pat. No. 5,658,727; U.S. Pat. No. 6,235,469; U.S. Pat. No. 5,969,108; U.S. Pat. No. 5,886,793].

Detailed Description of Methods to Generate Anti-CNGH0010 Antibodies

At least one anti-CNGH0010 antibody of the present invention can be optionally produced by a cell line, a mixed cell line, an immortalized cell or clonal population of immortalized cells, as well known in the art. See, e.g., Ausubel, et al., ed., Current Protocols in Molecular Biology, John Wiley & Sons, Inc., NY, N.Y. (1987-2001); Sambrook, et al., Molecular Cloning: A Laboratory Manual, 2nd Edition, Cold Spring Harbor, N.Y. (1989); Harlow and Lane, antibodies, a Laboratory Manual, Cold Spring Harbor, N.Y. (1989); Colligan, et al., eds., Current Protocols in Immunology, John Wiley & Sons, Inc., NY (1994-2001); Colligan et al., Current Protocols in Protein Science, John Wiley & Sons, NY, N.Y., (1997-2001), each entirely incorporated herein by reference.

Human antibodies that are specific for human CNGH0010 proteins (as described herein), variants, or fragments thereof can be raised against an appropriate immunogenic antigen as described herein, such as the isolated and/or CNGH0010 proteins, variants, or portions thereof (including synthetic molecules, such as synthetic polypeptides) as described herein. Other specific or general mammalian antibodies can be similarly raised. Preparation of immunogenic antigens, and monoclonal antibody production can be performed using any suitable technique.

In one approach, a hybridoma is produced by fusing a suitable immortal cell line, e.g., a myeloma cell line such as, but not limited to, Sp2/0, Sp2/0-AG14, NSO, NS1, NS2, AE-1, L.5, >243, P3X63Ag8.653, Sp2 SA3, Sp2 MAI, Sp2 SS1, Sp2 SA5, U937, MLA 144, ACT IV, MOLT4, DA-1, JURKAT, WEHI, K-562, COS, RAJI, NIH 3T3, HL-60, MLA 144, NAMAIWA, NEURO 2A, or the like, heteromylomas, fusion products thereof, any cell or fusion cell derived therefrom, or any other suitable cell line as known in the art (See, e.g., www.atcc.org, www.lifetech.com., and the like), with antibody producing cells, such as, but not limited to, isolated or cloned spleen, peripheral blood, lymph, tonsil, or other immune or B cell containing cells, or any other cells expressing heavy or light chain constant or variable or framework or CDR sequences, either as endogenous or heterologous nucleic acid molecule, as recombinant or endogenous, viral, bacterial, algal, prokaryotic, amphibian, insect, reptilian, fish, mammalian, rodent, equine, ovine, goat, sheep, primate, eukaryotic, genomic DNA, cDNA, rDNA, mitochondrial DNA or RNA, chloroplast DNA or RNA, hnRNA, mRNA, tRNA, single, double or triple stranded, hybridized, and the like or any combination thereof. See, e.g., Ausubel, supra, and Colligan, Immunology, supra, chapter 2, entirely incorporated herein by reference.

Antibody producing cells can also be obtained from the peripheral blood or, preferably the spleen or lymph nodes, of humans or other suitable animals that have been immunized with the antigen of interest. Any other suitable host cell can also be used for expressing heterologous or endogenous nucleic acid encoding an antibody, specified fragment or variant thereof, of the present invention. The fused cells (hybridomas) or recombinant cells can be isolated using selective culture conditions or other suitable known methods, and cloned by limiting dilution or cell sorting, or other known methods. Cells that produce antibodies with the desired specificity can be selected by a suitable assay (e.g., ELISA).

Other suitable methods of producing or isolating antibodies of the requisite specificity can be used, including, but not limited to, methods that select recombinant antibody from a polypeptide or protein display library (e.g., but not limited to, a bacteriophage, ribosome, oligonucleotide, RNA, cDNA, or the like, display library; e.g., as available from Cambridge antibody Technologies, Cambridgeshire, UK; MorphoSys, Martinsreid/Planegg, Del.; Biovation, Aberdeen, Scotland, UK; BioInvent, Lund, Sweden; Dyax Corp., Enzon, Affymax/Biosite; Xoma, Berkeley, Calif.; Ixsys. See, e.g., EP 368,684, PCT/GB91/01134; PCT/GB92/01755; PCT/GB92/002240; PCT/GB92/00883; PCT/GB93/00605; U.S. Ser. No. 08/350,260(May 12, 1994); PCT/GB94/01422; PCT/GB94/02662; PCT/GB97/01835; (CAT/MRC); WO90/14443; WO90/14424; WO90/14430; PCT/US94/1234; WO92/18619; WO96/07754; (Scripps); WO96/13583, WO97/08320 (MorphoSys); WO95/16027 (BioInvent); WO88/06630; WO90/3809 (Dyax); U.S. Pat. No. 4,704,692 (Enzon); PCT/US91/02989 (Affymax); WO89/06283; EP 371 998; EP 550 400; (Xoma); EP 229 046; PCT/US91/07149 (Ixsys); or stochastically generated peptides or proteins—U.S. Pat. Nos. 5,723,323, 5,763,192, 5,814,476, 5,817,483, 5,824,514, 5,976,862, WO 86/05803, EP 590 689 (Ixsys, now Applied Molecular Evolution (AME), each entirely incorporated herein by reference) or that rely upon immunization of transgenic animals (e.g., SCID mice, Nguyen et al., Microbiol. Immunol. 41:901-907 (1997); Sandhu et al., Crit. Rev. Biotechnol. 16:95-118 (1996); Eren et al., Immunol. 93:154-161 (1998), each entirely incorporated by reference as well as related patents and applications) that are capable of producing a repertoire of human antibodies, as known in the art and/or as described herein. Such techniques, include, but are not limited to, ribosome display (Hanes et al., Proc. Natl. Acad. Sci. USA, 94:4937-4942 (May 1997); Hanes et al., Proc. Natl. Acad. Sci. USA, 95:14130-14135 (November 1998)); single cell antibody producing technologies (e.g., selected lymphocyte antibody method (“SLAM”) (U.S. Pat. No. 5,627,052, Wen et al., J. Immunol. 17:887-892 (1987); Babcook et al., Proc. Natl. Acad. Sci. USA 93:7843-7848 (1996)); gel microdroplet and flow cytometry (Powell et al., Biotechnol. 8:333-337 (1990); One Cell Systems, Cambridge, Mass.; Gray et al., J. Imm. Meth. 182:155-163 (1995); Kenny et al., Bio/Technol. 13:787-790 (1995)); B-cell selection (Steenbakkers et al., Molec. Biol. Reports 19:125-134 (1994); Jonak et al., Progress Biotech, Vol. 5, In Vitro Immunization in Hybridoma Technology, Borrebaeck, ed., Elsevier Science Publishers B.V., Amsterdam, Netherlands (1988)).

Methods for engineering or humanizing non-human or human antibodies can also be used and are well known in the art. Generally, a humanized or engineered antibody has one or more amino acid residues from a source that is non-human, e.g., but not limited to, mouse, rat, rabbit, non-human primate or other mammal. These human amino acid residues are often referred to as “import” residues, which are typically taken from an “import” variable, constant or other domain of a known human sequence. Known human Ig sequences are disclosed, e.g., at www.ncbi.nlm.nih.gov/entrez/query.fcgi; www.atcc.org/phage/hdb.html; www.sciquest.com/; www.abcam.com/; www.antibodyresource.com/onlinecomp.html; www.public.iastate.edu/˜pedro/research_tools.html; www.mgen.uni-heidelberg.de/SD/IT/IT.html; www.whfreeman.com/immunology/CH05/kuby05.htm; www.library.thinkquest.org/12429/Immune/Antibody.html; www.hhmi.org/grants/lectures/1996/vlab/; www.path.cam.ac.uk/˜mrc7/mikeimages.html; www.antibodyresource.com/; mcb.harvard.edu/BioLinks/Immunology.html.www.immunologylink.com; pathbox.wustl.edu/˜hcenter/index.html; www.biotech.ufl.edu/˜hcl/; www.pebio.com/pa/340913/340913.html; www.nal.usda.gov/awic/pubs/antibody/; www.m.ehime-u.ac.jp/˜yasuhito/Elisa.html; www.biodesign.com/table.asp; www.icnet.uk/axp/facs/davies/links.html; www.biotech.ufl.edu/˜fccl/protocol.html; www.isac-net.org/sites_geo.html; aximtl.imt.uni-marburg.de/˜rek/AEPStart.html; baserv.uci.kun.nl/˜jraats/linksl.html; www.recab.uni-hd.de/immuno.bme.nwu.edu/; www.mrc-cpe.cam. ac.uk/imt-doc/public/INTRO.html; www.ibt.unam.mx/vir/V_mice.html; imgt.cnusc.fr:8104/; www.biochem.ucl.ac.uk/˜martin/abs/index.html; antibody.bath.ac.uk/; abgen.cvm.tamu.edu/lab/wwwabgen.html; www.unizh.ch/˜honegger/AHOseminar/Slide01.html; www.cryst.bbk.ac.uk/˜ubcg07s/; www.nimr.mrc.ac.uk/CC/ccaewg/ccaewg.htm; www.path.cam.ac.uk/˜mrc7/humanisation/TAHHP.html; www.ibt.unam.mx/vir/structure/stat_aim.html; www.biosci.missouri. edu/smithgp/index.html; www.cryst.bioc.cam.ac.uk/˜fmolina/Web-pages/Pept/spottech.html; www.jerini.de/fr_products.htm; www.patents.ibm.com/ibm.html.Kabat et al., Sequences of Proteins of Immunological Interest, U.S. Dept. Health (1983), each entirely incorporated herein by reference.

Such imported sequences can be used to reduce immunogenicity or reduce, enhance or modify binding, affinity, on-rate, off-rate, avidity, specificity, half-life, or any other suitable characteristic, as known in the art. Generally part or all of the non-human or human CDR sequences are maintained while the non-human sequences of the variable and constant regions are replaced with human or other amino acids. Antibodies can also optionally be humanized with retention of high affinity for the antigen and other favorable biological properties. To achieve this goal, humanized antibodies can be optionally prepared by a process of analysis of the parental sequences and various conceptual humanized products using three-dimensional models of the parental and humanized sequences. Three-dimensional immunoglobulin models are commonly available and are familiar to those skilled in the art. Computer programs are available which illustrate and display probable three-dimensional conformational structures of selected candidate immunoglobulin sequences. Inspection of these displays permits analysis of the likely role of the residues in the functioning of the candidate immunoglobulin sequence, i.e., the analysis of residues that influence the ability of the candidate immunoglobulin to bind its antigen. In this way, FR residues can be selected and combined from the consensus and import sequences so that the desired antibody characteristic, such as increased affinity for the target antigen(s), is achieved. In general, the CDR residues are directly and most substantially involved in influencing antigen binding. Humanization or engineering of antibodies of the present invention can be performed using any known method, such as but not limited to, those described in, Winter (Jones et al., Nature 321:522 (1986); Riechmann et al., Nature 332:323 (1988); Verhoeyen et al., Science 239:1534 (1988)), Sims et al., J. Immunol. 151: 2296 (1993); Chothia and Lesk, J. Mol. Biol. 196:901 (1987), Carter et al., Proc. Natl. Acad. Sci. U.S.A. 89:4285 (1992); Presta et al., J. Immunol. 151:2623 (1993), U.S. Pat. Nos. 5,723,323, 5,976,862, 5,824,514, 5,817,483, 5,814,476, 5,763,192, 5,723,323, 5,766,886, 5,714,352, 6,204,023, 6,180,370, 5,693,762, 5,530,101, 5,585,089, 5,225,539; and 4,816,567, PCT/: US98/16280, US96/18978, US91/09630, US91/05939, US94/01234, GB89/01334, GB91/01134, GB92/01755; WO90/14443, WO90/14424, WO90/14430, and EP 229246, each entirely incorporated herein by reference, included references cited therein.

The anti-CNGH0010 antibody can also be optionally generated by immunization of a transgenic animal (e.g., mouse, rat, hamster, non-human primate, and the like) capable of producing a repertoire of human antibodies, as described herein and/or as known in the art. Cells that produce a human anti-CNGH0010 antibody can be isolated from such animals and immortalized using suitable methods, such as the methods described herein.

Transgenic mice that can produce a repertoire of human antibodies that bind to human antigens can be produced by known methods (e.g., but not limited to, U.S. Pat. Nos. 5,770,428, 5,569,825, 5,545,806, 5,625,126, 5,625,825, 5,633,425, 5,661,016 and 5,789,650 issued to Lonberg et al.; Jakobovits et al. WO 98/50433, Jakobovits et al. WO 98/24893, Lonberg et al. WO 98/24884, Lonberg et al. WO 97/13852, Lonberg et al. WO 94/25585, Kucherlapate et al. WO 96/34096, Kucherlapate et al. EP 0463 151 B1, Kucherlapate et al. EP 0710 719 A1, Surani et al. U.S. Pat. No. 5,545,807, Bruggemann et al. WO 90/04036, Bruggemann et al. EP 0438 474 B1, Lonberg et al. EP 0814 259 A2, Lonberg et al. GB 2 272 440 A, Lonberg et al. Nature 368:856-859 (1994), Taylor et al., Int. Immunol. 6(4)579-591 (1994), Green et al, Nature Genetics 7:13-21 (1994), Mendez et al., Nature Genetics 15:146-156 (1997), Taylor et al., Nucleic Acids Research 20(23):6287-6295 (1992), Tuaillon et al., Proc Natl Acad Sci USA 90(8)3720-3724 (1993), Lonberg et al., Int Rev Immunol 13(1):65-93 (1995) and Fishwald et al., Nat Biotechnol 14(7):845-851 (1996), which are each entirely incorporated herein by reference). Generally, these mice comprise at least one transgene comprising DNA from at least one human immunoglobulin locus that is functionally rearranged, or which can undergo functional rearrangement. The endogenous immunoglobulin loci in such mice can be disrupted or deleted to eliminate the capacity of the animal to produce antibodies encoded by endogenous genes.

Screening antibodies for specific binding to similar proteins or fragments can be conveniently achieved using peptide display libraries. This method involves the screening of large collections of peptides for individual members having the desired function or structure. Antibody screening of peptide display libraries is well known in the art. The displayed peptide sequences can be from 3 to 5,000 or more amino acids in length, frequently from 5-100 amino acids long, and often from about 8 to 25 amino acids long. In addition to direct chemical synthetic methods for generating peptide libraries, several recombinant DNA methods have been described. One type involves the display of a peptide sequence on the surface of a bacteriophage or cell. Each bacteriophage or cell contains the nucleotide sequence encoding the particular displayed peptide sequence. Such methods are described in PCT Patent Publication Nos. 91/17271, 91/18980, 91/19818, and 93/08278. Other systems for generating libraries of peptides have aspects of both in vitro chemical synthesis and recombinant methods. See, PCT Patent Publication Nos. 92/05258, 92/14843, and 96/19256. See also, U.S. Pat. Nos. 5,658,754 and 5,643,768. Peptide display libraries, vector, and screening kits are commercially available from such suppliers as Invitrogen (Carlsbad, Calif.), and Cambridge antibody Technologies (Cambridgeshire, UK). See, e.g., U.S. Pat. Nos. 4,704,692, 4,939,666, 4,946,778, 5,260,203, 5,455,030, 5,518,889, 5,534,621, 5,656,730, 5,763,733, 5,767,260, 5,856,456, assigned to Enzon; 5,223,409, 5,403,484, 5,571,698, 5,837,500, assigned to Dyax, 5,427,908, 5,580,717, assigned to Affymax; 5,885,793, assigned to Cambridge antibody Technologies; 5,750,373, assigned to Genentech, 5,618,920, 5,595,898, 5,576,195, 5,698,435, 5,693,493, and 5,698,417, assigned to Xoma, Colligan, supra; Ausubel, supra; or Sambrook, supra, each of the above patents and publications entirely incorporated herein by reference.

Antibodies of the present invention can also be prepared in milk by administering at least one anti-CNGH0010 antibody encoding nucleic acid to transgenic animals or mammals, such as goats, cows, horses, sheep, and the like, that produce antibodies in their milk. Such animals can be provided using known methods. See, e.g., but not limited to, U.S. Pat. Nos. 5,827,690; 5,849,992; 4,873,316; 5,849,992; 5,994,616; 5,565,362; 5,304,489, and the like, each of which is entirely incorporated herein by reference.

Antibodies of the present invention can additionally be prepared using at least one anti-CNGH0010 antibody encoding nucleic acid to provide transgenic plants and cultured plant cells (e.g., but not limited to, tobacco and maize) that produce such antibodies, specified portions or variants in the plant parts or in cells cultured therefrom. As a non-limiting example, transgenic tobacco leaves expressing recombinant proteins have been successfully used to provide large amounts of recombinant proteins, e.g., using an inducible promoter. See, e.g., Cramer et al., Curr. Top. Microbol. Immunol. 240:95-118 (1999) and references cited therein. Also, transgenic maize has been used to express mammalian proteins at commercial production levels, with biological activities equivalent to those produced in other recombinant systems or purified from natural sources. See, e.g., Hood et al., Adv. Exp. Med. Biol. 464:127-147 (1999) and references cited therein. Antibodies have also been produced in large amounts from transgenic plant seeds including antibody fragments, such as single chain antibodies (scFv's), including tobacco seeds and potato tubers. See, e.g., Conrad et al., Plant Mol. Biol. 38:101-109 (1998) and reference cited therein. Thus, antibodies of the present invention can also be produced using transgenic plants, according to known methods. See also, e.g., Fischer et al., Biotechnol. Appl. Biochem. 30:99-108 (October, 1999), Ma et al., Trends Biotechnol. 13:522-7 (1995); Ma et al., Plant Physiol. 109:341-6 (1995); Whitelam et al., Biochem. Soc. Trans. 22:940-944 (1994); and references cited therein. Each of the above references is entirely incorporated herein by reference.

The antibodies of the invention can bind human CNGH0010 with a wide range of affinities (KD). In a preferred embodiment, at least one human mAb of the present invention can optionally bind human CNGH0010 with high affinity. For example, a human mAb can bind human CNGH0010 with a KD equal to or less than about 10⁻⁷ M, such as but not limited to, 0.1-9.9 (or any range or value therein) X 10⁻⁷, 10⁻⁸, 10⁻⁹, 10⁻¹⁰, 10⁻¹¹, 10⁻¹², 10⁻¹³ or any range or value therein.

The affinity or avidity of an antibody for an antigen can be determined experimentally using any suitable method. (See, for example, Berzofsky, et al., “Antibody-Antigen Interactions,” In Fundamental Immunology, Paul, W. E., Ed., Raven Press: New York, N.Y. (1984); Kuby, Janis Immunology, W. H. Freeman and Company: New York, N.Y. (1992); and methods described herein). The measured affinity of a particular antibody-antigen interaction can vary if measured under different conditions (e.g., salt concentration, pH). Thus, measurements of affinity and other antigen-binding parameters (e.g., K_(D), K_(a), K_(d)) are preferably made with standardized solutions of antibody and antigen, and a standardized buffer, such as the buffer described herein.

Purification of an Antibody

An anti-CNGH0010 antibody can be recovered and purified from recombinant cell cultures by well-known methods including, but not limited to, protein A purification, ammonium sulfate or ethanol precipitation, acid extraction, anion or cation exchange chromatography, phosphocellulose chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite chromatography and lectin chromatography. High performance liquid chromatography (“HPLC”) can also be employed for purification. See, e.g., Colligan, Current Protocols in Immunology, or Current Protocols in Protein Science, John Wiley & Sons, NY, N.Y., (1997-2001), e.g., Chapters 1, 4, 6, 8, 9, 10, each entirely incorporated herein by reference.

Antibodies of the present invention include naturally purified products, products of chemical synthetic procedures, and products produced by recombinant techniques from a eukaryotic host, including, for example, yeast, higher plant, insect and mammalian cells. Depending upon the host employed in a recombinant production procedure, the antibody of the present invention can be glycosylated or can be non-glycosylated, with glycosylated preferred. Such methods are described in many standard laboratory manuals, such as Sambrook, supra, Sections 17.37-17.42; Ausubel, supra, Chapters 10, 12, 13, 16, 18 and 20, Colligan, Protein Science, supra, Chapters 12-14, all entirely incorporated herein by reference.

Cloning and Expression of anti-CNGH0010 Antibody in Mammalian Cells

A typical mammalian expression vector contains at least one promoter element, which mediates the initiation of transcription of mRNA, the antibody coding sequence, and signals required for the termination of transcription and polyadenylation of the transcript. Additional elements include enhancers, Kozak sequences, and intervening sequences flanked by donor and acceptor sites for RNA splicing. Highly efficient transcription can be achieved with the early and late promoters from SV40, the long terminal repeats (LTRS) from Retroviruses, e.g., GAS-6, HTLVI, HIVI and the early promoter of the cytomegalovirus (CMV). However, cellular elements can also be used (e.g., the human actin promoter). Suitable expression vectors for use in practicing the present invention include, for example, vectors such as pIRES1neo, pRetro-Off, pRetro-On, PLXSN, or pLNCX (Clonetech Labs, Palo Alto, Calif.), pcDNA3.1 (+/−), pcDNA/Zeo (+/−) or pcDNA3.1/Hygro (+/−) (Invitrogen), PSVL and PMSG (Pharmacia, Uppsala, Sweden), pGAS-6cat (ATCC 37152), pSV2dhfr (ATCC 37146) and pBC12MI (ATCC 67109). Mammalian host cells that could be used include human Hela 293, H9 and Jurkat cells, mouse NIH3T3 and C127 cells, Cos 1, Cos 7 and CV 1, quail QC1-3 cells, mouse L cells and Chinese hamster ovary (CHO) cells.

Alternatively, the gene can be expressed in stable cell lines that contain the gene integrated into a chromosome. The co-transfection with a selectable marker such as dhfr, gpt, neomycin, or hygromycin allows the identification and isolation of the transfected cells.

The transfected gene can also be amplified to express large amounts of the encoded antibody. The DHFR (dihydrofolate reductase) marker is useful to develop cell lines that carry several hundred or even several thousand copies of the gene of interest. Another useful selection marker is the enzyme glutamine synthase (GS) (Murphy, et al., Biochem. J. 227:277-279 (1991); Bebbington, et al., Bio/Technology 10:169-175 (1992)). Using these markers, the mammalian cells are grown in selective medium and the cells with the highest resistance are selected. These cell lines contain the amplified gene(s) integrated into a chromosome. Chinese hamster ovary (CHO) and NSO cells are often used for the production of antibodies.

The expression vectors pC1 and pC4 contain the strong promoter (LTR) of the Rous Sarcoma Virus (Cullen, et al., Molec. Cell. Biol. 5:438-447 (1985)) plus a fragment of the CMV-enhancer (Boshart, et al., Cell 41:521-530 (1985)). Multiple cloning sites, e.g., with the restriction enzyme cleavage sites BamHI, XbaI and Asp718, facilitate the cloning of the gene of interest. The vectors contain in addition the 3′ intron, the polyadenylation and termination signal of the rat preproinsulin gene.

Anti-Idiotype Antibodies to Anti-CNGH0010 Antibody Compositions

In addition to monoclonal or chimeric anti-CNGH0010 antibodies, the present invention is also directed to an anti-idiotypic (anti-Id) antibody specific for such antibodies of the invention. An anti-Id antibody is an antibody that recognizes unique determinants generally associated with the antigen-binding region of another antibody. The anti-Id can be prepared by immunizing an animal of the same species and genetic type (e.g., mouse strain) as the source of the Id antibody with the antibody or a CDR containing region thereof. The immunized animal will recognize and respond to the idiotypic determinants of the immunizing antibody and produce an anti-Id antibody. The anti-Id antibody may also be used as an “immunogen” to induce an immune response in yet another animal, producing a so-called anti-anti-Id antibody.

CNGH0010 Polypeptide or Antibody Compositions

The present invention also provides CNGH0010 polypeptide or CNGH0010 antibody compositions comprising at least one CNGH0010 polypeptide or CNGH0010 antibodies as described herein that are provided in a non-naturally occurring composition, mixture or form. Such compositions comprise non-naturally occurring compositions comprising at least one or two full length, C- and/or N-terminally deleted variants, domains, fragments, or specified variants, of the CNGH0010 polypeptide amino acid sequence selected from the group consisting of 80-100% of the contiguous amino acids of SEQ ID NOS:3, 5, 7, 9, 11, and 41, or CNGH0010 antibody or specified fragments, domains or variants thereof, optionally, in combination with a pharmaceutically acceptable carrier or diluent.

CNGH0010 polypeptides or antibody compounds, compositions or combinations of the present invention can further comprise at least one of any suitable auxiliary, such as, but not limited to, diluent, binder, stabilizer, buffers, salts, lipophilic solvents, preservative, adjuvant or the like. Pharmaceutically acceptable auxiliaries are preferred. Non-limiting examples of, and methods of preparing such sterile solutions are well known in the art, such as, but limited to, Gennaro, Ed., Remington's Pharmaceutical Sciences, 18th Edition, Mack Publishing Co. (Easton, Pa.) 1990. Pharmaceutically acceptable carriers can be routinely selected that are suitable for the mode of administration, solubility and/or stability of the anti-CNGH0010 antibody, fragment or variant composition as well known in the art or as described herein.

Pharmaceutical excipients and additives useful in the present composition include, but are not limited to, proteins, polypeptides, amino acids, lipids, and carbohydrates (e.g., sugars, including monosaccharides, di-, tri-, tetra-, and oligosaccharides; derivatized sugars such as alditols, aldonic acids, esterified sugars and the like; and polysaccharides or sugar polymers), which can be present singly or in combination, comprising alone or in combination 1-99.99% by weight or volume. Exemplary protein excipients include serum albumin such as human serum albumin (HSA), recombinant human albumin (rHA), gelatin, casein, and the like. Representative amino acid/antibody components, which can also function in a buffering capacity, include alanine, glycine, arginine, betaine, histidine, glutamic acid, aspartic acid, cysteine, lysine, leucine, isoleucine, valine, methionine, phenylalanine, aspartame, and the like. One preferred amino acid is glycine.

Carbohydrate excipients suitable for use in the invention include, for example, monosaccharides, such as fructose, maltose, galactose, glucose, D-mannose, sorbose, and the like; disaccharides, such as lactose, sucrose, trehalose, cellobiose, and the like; polysaccharides, such as raffinose, melezitose, maltodextrins, dextrans, starches, and the like; and alditols, such as mannitol, xylitol, maltitol, lactitol, xylitol sorbitol (glucitol), myoinositol and the like. Preferred carbohydrate excipients for use in the present invention are mannitol, trehalose, and raffinose.

Anti-CNGH0010 polypeptide or antibody compositions can also include a buffer or a pH-adjusting agent; typically, the buffer is a salt prepared from an organic acid or base. Representative buffers include organic acid salts, such as salts of citric acid, ascorbic acid, gluconic acid, carbonic acid, tartaric acid, succinic acid, acetic acid, or phthalic acid; Tris, tromethamine hydrochloride, or phosphate buffers. Preferred buffers for use in the present compositions are organic acid salts such as citrate.

Additionally, anti-CNGH0010 antibody compositions of the invention can include polymeric excipients/additives, such as polyvinylpyrrolidones, ficolls (a polymeric sugar), dextrates (e.g., cyclodextrins, such as 2-hydroxypropyl-β-cyclodextrin), polyethylene glycols, flavoring agents, antimicrobial agents, sweeteners, antioxidants, antistatic agents, surfactants (e.g., polysorbates such as “TWEEN 20” and “TWEEN 80”), lipids (e.g., phospholipids, fatty acids), steroids (e.g., cholesterol), and chelating agents (e.g., EDTA).

These and additional known pharmaceutical excipients and/or additives suitable for use in the anti-CNGH0010 antibody, portion or variant compositions according to the invention are known in the art, e.g., as listed in “Remington: The Science & Practice of Pharmacy”, 19th ed., Williams & Williams, (1995), and in the “Physician's Desk Reference”, 52nd ed., Medical Economics, Montvale, N.J. (1998), the disclosures of which are entirely incorporated herein by reference. Preferred carrier or excipient materials are carbohydrates (e.g., saccharides and alditols) and buffers (e.g., citrate) or polymeric agents.

Anti-CNGH0010 antibody compositions of the present invention can further comprise at least one of any suitable and effective amount of a composition or pharmaceutical composition comprising at least one anti-CNGH0010 antibody contacting or administering to a cell, tissue, organ, animal or patient in need of such modulation, treatment or therapy, optionally, further comprising at least one selected from at least one TNF antagonist (e.g., but not limited to a TNF antibody or fragment, a soluble TNF receptor or fragment, fusion proteins thereof, or a small molecule TNF antagonist), an antirheumatic (e.g., methotrexate, auranofin, aurothioglucose, azathioprine, etanercept, gold sodium thiomalate, hydroxychloroquine sulfate, leflunomide, sulfasalzine), a muscle relaxant, a narcotic, a non-steroid anti-inflammatory drug (NSAID), an analgesic, an anesthetic, a sedative, a local anesthetic, a neuromuscular blocker, an antimicrobial (e.g., aminoglycoside, an antifungal, an antiparasitic, an antiviral, a carbapenem, cephalosporin, a fluororquino lone, a macro lide, a penicillin, a sulfonamide, a tetracycline, another antimicrobial), an antipsoriatic, a corticosteriod, an anabolic steroid, a diabetes related agent, a mineral, a nutritional, a thyroid agent, a vitamin, a calcium related hormone, an antidiarrheal, an antitussive, an antiemetic, an antiulcer, a laxative, an anticoagulant, an erythropoietin (e.g., epoetin alpha), a filgrastim (e.g., G-CSF, Neupogen), a sargramostim (GM-CSF, Leukine), an immunization, an immunoglobulin, an immunosuppressive (e.g., basiliximab, cyclosporine, daclizumab), a growth hormone, a hormone replacement drug, an estrogen receptor modulator, a mydriatic, a cycloplegic, an alkylating agent, an antimetabolite, a mitotic inhibitor, a radiopharmaceutical, an antidepressant, antimanic agent, an antipsychotic, an anxiolytic, a hypnotic, a sympathomimetic, a stimulant, donepezil, tacrine, an asthma medication, a beta agonist, an inhaled steroid, a leukotriene inhibitor, a methylxanthine, a cromolyn, an epinephrine or analog, domase alpha (Pulmozyme), a cytokine or a cytokine antagonist. Non-limiting examples of such cytokines include, but are not limited to, any of the interleukins from IL-1 to IL-29. Suitable dosages are well known in the art. See, e.g., Wells et al., eds., Pharmacotherapy Handbook, 2nd Edition, Appleton and Lange, Stamford, Conn. (2000); PDR Pharmacopoeia, Tarascon Pocket Pharmacopoeia 2000, Deluxe Edition, Tarascon Publishing, Loma Linda, Calif. (2000), each of which references are entirely incorporated herein by reference.

Such anti-cancer or anti-infectives can also include toxin molecules that are associated, bound, co-formulated or co-administered with at least one antibody of the present invention. The toxin can optionally act to selectively kill the pathologic cell or tissue. The pathologic cell can be a cancer or other cell. Such toxins can be, but are not limited to, purified or recombinant toxin or toxin fragment comprising at least one functional cytotoxic domain of toxin, e.g., selected from at least one of ricin, diphtheria toxin, a venom toxin, or a bacterial toxin. The term toxin also includes both endotoxins and exotoxins produced by any naturally occurring, mutant or recombinant bacteria or viruses which may cause any pathological condition in humans and other mammals, including toxin shock, which can result in death. Such toxins may include, but are not limited to, enterotoxigenic E. coli heat-labile enterotoxin (LT), heat-stable enterotoxin (ST), Shigella cytotoxin, Aeromonas enterotoxins, toxic shock syndrome toxin-1 (TSST-1), Staphylococcal enterotoxin A (SEA), B (SEB), or C (SEC), Streptococcal enterotoxins and the like. Such bacteria include, but are not limited to, strains of a species of enterotoxigenic E. coli (ETEC), enterohemorrhagic E. coli (e.g., strains of serotype 0157:H7), Staphylococcus species (e.g., Staphylococcus aureus, Staphylococcus pyogenes), Shigella species (e.g., Shigella dysenteriae, Shigella flexneri, Shigella boydii, and Shigella sonnei), Salmonella species (e.g., Salmonella typhi, Salmonella cholera-suis, Salmonella enteritidis), Clostridium species (e.g., Clostridium perfringens, Clostridium dificile, Clostridium botulinum), Camphlobacter species (e.g., Camphlobacter jejuni, Camphlobacter fetus), Heliobacter species, (e.g., Heliobacter pylori), Aeromonas species (e.g., Aeromonas sobria, Aeromonas hydrophila, Aeromonas caviae), Pleisomonas shigelloides, Yersina enterocolitica, Vibrios species (e.g., Vibrios cholerae, Vibrios parahemolyticus), Klebsiella species, Pseudomonas aeruginosa, and Streptococci. See, e.g., Stein, ed., INTERNAL MEDICINE, 3rd ed., pp 1-13, Little, Brown and Co., Boston, (1990); Evans et al., eds., Bacterial Infections of Humans: Epidemiology and Control, 2d. Ed., pp 239-254, Plenum Medical Book Co., New York (1991); Mandell et al, Principles and Practice of Infectious Diseases, 3d. Ed., Churchill Livingstone, N.Y. (1990); Berkow et al, eds., The Merck Manual, 16th edition, Merck and Co., Rahway, N.J., 1992; Wood et al, FEMS Microbiology Immunology, 76:121-134 (1991); Marrack et al, Science, 248:705-711 (1990), the contents of which references are incorporated entirely herein by reference.

Applications

The present invention provides a method for modulating or treating at least one CNGH0010 related disease, in a cell, tissue, organ, animal, or patient, as known in the art or as described herein, using at least one CNGH0010 polypeptide or CNGH0010 antibody of the present invention.

Compositions of CNGH0010 binding polypeptides or CNGH0010 antibody or polypeptide antagonists may find therapeutic use in the treatment of disease conditions such as cancer or other human diseases with deregulated matrix production and remodeling, including lung fibrosis, liver cirrhosis, osteoporosis, rheumatoid arthritis, and asthma. Potential disease indications may also include diseases with defects in cell mechanics, tissure structure, or deregulation of mechanochemical conversion caused by pathological alteration of matrix (Ingber D., Mechanolbiology and diseases of mechanotransduction, Annals of Medicine, in press).

The present invention also provides a method for modulating or treating at least one immune related disease, in a cell, tissue, organ, animal, or patient including, but not limited to, at least one of rheumatoid arthritis, juvenile rheumatoid arthritis, systemic onset juvenile rheumatoid arthritis, psoriatic arthritis, ankylosing spondilitis, gastric ulcer, seronegative arthropathies, osteoarthritis, inflammatory bowel disease, ulcerative colitis, systemic lupus erythematosis, antiphospholipid syndrome, iridocyclitis/uveitis/optic neuritis, idiopathic pulmonary fibrosis, systemic vasculitis/wegener's granulomatosis, sarcoidosis, orchitis/vasectomy reversal procedures, allergic/atopic diseases, asthma, allergic rhinitis, eczema, allergic contact dermatitis, allergic conjunctivitis, hypersensitivity pneumonitis, transplants, organ transplant rejection, graft-versus-host disease, systemic inflammatory response syndrome, sepsis syndrome, gram positive sepsis, gram negative sepsis, culture negative sepsis, fungal sepsis, neutropenic fever, urosepsis, meningococcemia, trauma/hemorrhage, burns, ionizing radiation exposure, acute pancreatitis, adult respiratory distress syndrome, rheumatoid arthritis, alcohol-induced hepatitis, chronic inflammatory pathologies, sarcoidosis, Crohn's pathology, sickle cell anemia, diabetes, nephrosis, atopic diseases, hypersensitity reactions, allergic rhinitis, hay fever, perennial rhinitis, conjunctivitis, endometriosis, asthma, urticaria, systemic anaphalaxis, dermatitis, pernicious anemia, hemolytic disease, thrombocytopenia, graft rejection of any organ or tissue, kidney translplant rejection, heart transplant rejection, liver transplant rejection, pancreas transplant rejection, lung transplant rejection, bone marrow transplant (BMT) rejection, skin allograft rejection, cartilage transplant rejection, bone graft rejection, small bowel transplant rejection, fetal thymus implant rejection, parathyroid transplant rejection, xenograft rejection of any organ or tissue, allograft rejection, anti-receptor hypersensitivity reactions, Graves disease, Raynoud's disease, type B insulin-resistant diabetes, asthma, myasthenia gravis, antibody-meditated cytotoxicity, type III hypersensitivity reactions, systemic lupus erythematosus, POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome), polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, skin changes syndrome, antiphospholipid syndrome, pemphigus, scleroderma, mixed connective tissue disease, idiopathic Addison's disease, diabetes mellitus, chronic active hepatitis, primary billiary cirrhosis, vitiligo, vasculitis, post-Ml cardiotomy syndrome, type IV hypersensitivity, contact dermatitis, hypersensitivity pneumonitis, allograft rejection, granulomas due to intracellular organisms, drug sensitivity, metabolic/idiopathic, Wilson's disease, hemachromatosis, alpha-1-antitrypsin deficiency, diabetic retinopathy, hashimoto's thyroiditis, osteoporosis, hypothalamic-pituitary-adrenal axis evaluation, primary biliary cirrhosis, thyroiditis, encephalomyelitis, cachexia, cystic fibrosis, neonatal chronic lung disease, chronic obstructive pulmonary disease (COPD), familial hematophagocytic lymphohistiocytosis, dermatologic conditions, psoriasis, alopecia, nephrotic syndrome, nephritis, glomerular nephritis, acute renal failure, hemodialysis, uremia, toxicity, preeclampsia, okt3 therapy, anti-cd3 therapy, cytokine therapy, chemotherapy, radiation therapy (e.g., including but not limited toasthenia, anemia, cachexia, and the like), chronic salicylate intoxication, and the like. See, e.g., the Merck Manual, 12th-17th Editions, Merck & Company, Rahway, N.J. (1972, 1977, 1982, 1987, 1992, 1999), Pharmacotherapy Handbook, Wells et al., eds., Second Edition, Appleton and Lange, Stamford, Conn. (1998, 2000), each entirely incorporated by reference.

The present invention also provides a method for modulating or treating at least one malignant disease in a cell, tissue, organ, animal or patient, including, but not limited to, at least one of: leukemia, acute leukemia, acute lymphoblastic leukemia (ALL), B-cell, T-cell or FAB ALL, acute myeloid leukemia (AML), chromic myelocytic leukemia (CML), chronic lymphocytic leukemia (CLL), hairy cell leukemia, myelodyplastic syndrome (MDS), a lymphoma, Hodgkin's disease, a malignamt lymphoma, non-hodgkin's lymphoma, Burkitt's lymphoma, multiple myeloma, Kaposi's sarcoma, colorectal carcinoma, pancreatic carcinoma, nasopharyngeal carcinoma, malignant histiocytosis, paraneoplastic syndrome/hypercalcemia of malignancy, solid tumors, adenocarcinomas, sarcomas, malignant melanoma, hemangioma, metastatic disease, cancer related bone resorption, cancer related bone pain, and the like.

Any method of the present invention can comprise administering an effective amount of a composition or pharmaceutical composition comprising at least one anti-CNGH0010 antibody to a cell, tissue, organ, animal, or patient in need of such modulation, treatment or therapy. Such a method can optionally further comprise co-administration or combination therapy for treating such immune diseases, wherein the administration of the CNGH0010 polypeptide or CNGH0010 antibody, specified portion or variant thereof, further comprises administering, before concurrently, and/or after, at least one selected from at least one TNF antagonist (e.g., but not limited to a TNF antibody or fragment, a soluble TNF receptor or fragment, fusion proteins thereof, or a small molecule TNF antagonist), an antirheumatic (e.g., methotrexate, auranofin, aurothioglucose, azathioprine, etanercept, gold sodium thiomalate, hydroxychloroquine sulfate, leflunomide, sulfasalzine), a muscle relaxant, a narcotic, a non-steroid anti-inflammatory drug (NSAID), an analgesic, an anesthetic, a sedative, a local anesthetic, a neuromuscular blocker, an antimicrobial (e.g., aminoglycoside, an antifungal, an antiparasitic, an antiviral, a carbapenem, cephalosporin, a fluororquino lone, a macro lide, a penicillin, a sulfonamide, a tetracycline, another antimicrobial), an antipsoriatic, a corticosteriod, an anabolic steroid, a diabetes related agent, a mineral, a nutritional, a thyroid agent, a vitamin, a calcium related hormone, an antidiarrheal, an antitussive, an antiemetic, an antiulcer, a laxative, an anticoagulant, an erythropoietin (e.g., epoetin alpha), a filgrastim (e.g., G-CSF, Neupogen), a sargramostim (GM-CSF, Leukine), an immunization, an immunoglobulin, an immunosuppressive (e.g., basiliximab, cyclosporine, daclizumab), a growth hormone, a hormone replacement drug, an estrogen receptor modulator, a mydriatic, a cycloplegic, an alkylating agent, an antimetabolite, a mitotic inhibitor, a radiopharmaceutical, an antidepressant, antimanic agent, an antipsychotic, an anxiolytic, a hypnotic, a sympathomimetic, a stimulant, donepezil, tacrine, an asthma medication, a beta agonist, an inhaled steroid, a leukotriene inhibitor, a methylxanthine, a cromolyn, an epinephrine or analog, domase alpha (Pulmozyme), a cytokine or a cytokine antagonist. Suitable dosages are well known in the art. See, e.g., Wells et al., eds., Pharmacotherapy Handbook, 2nd Edition, Appleton and Lange, Stamford, Conn. (2000); PDR Pharmacopoeia, Tarascon Pocket Pharmacopoeia 2000, Deluxe Edition, Tarascon Publishing, Loma Linda, Calif. (2000), each of which references are entirely incorporated herein by reference.

Typically, treatment of pathologic conditions is effected by administering an effective amount or dosage of at least one anti-CNGH0010 antibody composition that total, on average, a range from at least about 0.01 to 500 milligrams of at least one anti-CNGH0010 antibody per kilogram of patient per dose, and, preferably, from at least about 0.1 to 100 milligrams antibody/kilogram of patient per single or multiple administration, depending upon the specific activity of contained in the composition. Alternatively, the effective serum concentration can comprise 0.1-5000 μg/ml serum concentration per single or multiple administration. Suitable dosages are known to medical practitioners and will, of course, depend upon the particular disease state, specific activity of the composition being administered, and the particular patient undergoing treatment. In some instances, to achieve the desired therapeutic amount, it can be necessary to provide for repeated administration, i.e., repeated individual administrations of a particular monitored or metered dose, where the individual administrations are repeated until the desired daily dose or effect is achieved.

Preferred doses can optionally include 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99 and/or 100-500 mg/kg/administration, or any range, value or fraction thereof, or to achieve a serum concentration of 0.1, 0.5, 0.9, 1.0, 1.1, 1.2, 1.5, 1.9, 2.0, 2.5, 2.9, 3.0, 3.5, 3.9, 4.0, 4.5, 4.9, 5.0, 5.5, 5.9, 6.0, 6.5, 6.9, 7.0, 7.5, 7.9, 8.0, 8.5, 8.9, 9.0, 9.5, 9.9, 10, 10.5, 10.9, 11, 11.5, 11.9, 20, 12.5, 12.9, 13.0, 13.5, 13.9, 14.0, 14.5, 4.9, 5.0, 5.5, 5.9, 6.0, 6.5, 6.9, 7.0, 7.5, 7.9, 8.0, 8.5, 8.9, 9.0, 9.5, 9.9, 10, 10.5, 10.9, 11, 11.5, 11.9, 12, 12.5, 12.9, 13.0, 13.5, 13.9, 14, 14.5, 15, 15.5, 15.9, 16, 16.5, 16.9, 17, 17.5, 17.9, 18, 18.5, 18.9, 19, 19.5, 19.9, 20, 20.5, 20.9, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 96, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, and/or 5000 μg/ml serum concentration per single or multiple administration, or any range, value or fraction thereof.

Alternatively, the dosage administered can vary depending upon known factors, such as the pharmacodynamic characteristics of the particular agent, and its mode and route of administration; age, health, and weight of the recipient; nature and extent of symptoms, kind of concurrent treatment, frequency of treatment, and the effect desired. Usually, a dosage of active ingredient can be about 0.1 to 100 milligrams per kilogram of body weight. Ordinarily 0.1 to 50, and preferably 0.1 to 10 milligrams per kilogram per administration or in sustained release form is effective to obtain desired results.

As a non-limiting example, treatment of humans or animals can be provided as a one-time or periodic dosage of at least one antibody of the present invention 0.1 to 100 mg/kg, such as 0.5, 0.9, 1.0, 1.1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 40, 45, 50, 60, 70, 80, 90 or 100 mg/kg, per day, on at least one of day 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, or 40, or alternatively or additionally, at least one of week 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, or 52, or alternatively or additionally, at least one of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 years, or any combination thereof, using single, infusion or repeated doses.

Dosage forms (composition) suitable for internal administration generally contain from about 0.1 milligram to about 500 milligrams of active ingredient per unit or container. In these pharmaceutical compositions, the active ingredient will ordinarily be present in an amount of about 0.5-99.999% by weight based on the total weight of the composition.

For parenteral administration, the antibody can be formulated as a solution, suspension, emulsion, particle, powder, or lyophilized powder in association, or separately provided, with a pharmaceutically acceptable parenteral vehicle. Examples of such vehicles are water, saline, Ringer's solution, dextrose solution, and 1-10% human serum albumin. Liposomes and nonaqueous vehicles, such as fixed oils, can also be used. The vehicle or lyophilized powder can contain additives that maintain isotonicity (e.g., sodium chloride, mannitol) and chemical stability (e.g., buffers and preservatives). The formulation is sterilized by known or suitable techniques.

Suitable pharmaceutical carriers are described in the most recent edition of Remington's Pharmaceutical Sciences, A. Osol, a standard reference text in this field.

Formulations

As noted above, the invention provides for stable formulations, which preferably contain a phosphate buffer with saline or a chosen salt, as well as preserved solutions and formulations containing a preservative as well as multi-use preserved formulations suitable for pharmaceutical or veterinary use, comprising at least one anti-CNGH0010 antibody in a pharmaceutically acceptable formulation. Preserved formulations contain at least one known preservative or optionally selected from the group consisting of at least one phenol, m-cresol, p-cresol, o-cresol, chlorocresol, benzyl alcohol, phenylmercuric nitrite, phenoxyethanol, formaldehyde, chlorobutanol, magnesium chloride (e.g., hexahydrate), alkylparaben (methyl, ethyl, propyl, butyl and the like), benzalkonium chloride, benzethonium chloride, sodium dehydroacetate and thimerosal, or mixtures thereof in an aqueous diluent. Any suitable concentration or mixture can be used as known in the art, such as 0.001-5%, or any range or value therein, such as, but not limited to, 0.001, 0.003, 0.005, 0.009, 0.01, 0.02, 0.03, 0.05, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3.0, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4.0, 4.3, 4.5, 4.6, 4.7, 4.8, 4.9, or any range or value therein. Non-limiting examples include, no preservative, 0.1-2% m-cresol (e.g., 0.2, 0.3, 0.4, 0.5, 0.9, 1.0%), 0.1-3% benzyl alcohol (e.g., 0.5, 0.9, 1.1, 1.5, 1.9, 2.0, 2.5%), 0.001-0.5% thimerosal (e.g., 0.005, 0.01), 0.001-2.0% phenol (e.g., 0.05, 0.25, 0.28, 0.5, 0.9, 1.0%), 0.0005-1.0% alkylparaben(s) (e.g., 0.00075, 0.0009, 0.001, 0.002, 0.005, 0.0075, 0.009, 0.01, 0.02, 0.05, 0.075, 0.09, 0.1, 0.2, 0.3, 0.5, 0.75, 0.9, 1.0%), and the like.

As noted above, the invention provides an article of manufacture, comprising packaging material and at least one vial comprising a solution of at least one anti-CNGH0010 antibody with the prescribed buffers and/or preservatives, optionally, in an aqueous diluent, wherein the packaging material comprises a label that indicates that such solution can be held over a period of 1, 2, 3, 4, 5, 6, 9, 12, 18, 20, 24, 30, 36, 40, 48, 54, 60, 66, 72 hours or greater. The invention further comprises an article of manufacture, comprising packaging material, a first vial comprising lyophilized at least one anti-CNGH0010 antibody, and a second vial comprising an aqueous diluent of prescribed buffer or preservative, wherein the packaging material comprises a label that instructs a patient to reconstitute the at least one anti-CNGH0010 antibody in the aqueous diluent to form a solution that can be held over a period of twenty-four hours or greater.

The at least one anti-CNGH0010 antibody used in accordance with the present invention can be produced by recombinant means, including from mammalian cell or transgenic preparations, or can be purified from other biological sources, as described herein or as known in the art.

The range of at least one anti-CNGH0010 antibody in the product of the present invention includes amounts yielding upon reconstitution, if in a wet/dry system, concentrations from about 1.0 μg/ml to about 1000 mg/ml, although lower and higher concentrations are operable and are dependent on the intended delivery vehicle, e.g., solution formulations will differ from transdermal patch, pulmonary, transmucosal, or osmotic or micro pump methods.

Preferably, the aqueous diluent optionally further comprises a pharmaceutically acceptable preservative. Preferred preservatives include those selected from the group consisting of phenol, m-cresol, p-cresol, o-cresol, chlorocresol, benzyl alcohol, alkylp arab en (methyl, ethyl, propyl, butyl and the like), benzalkonium chloride, benzethonium chloride, sodium dehydroacetate and thimerosal, or mixtures thereof. The concentration of preservative used in the formulation is a concentration sufficient to yield an anti-microbial effect. Such concentrations are dependent on the preservative selected and are readily determined by the skilled artisan.

Other excipients, e.g., isotonicity agents, buffers, antioxidants, preservative enhancers, can be optionally and preferably added to the diluent. An isotonicity agent, such as glycerin, is commonly used at known concentrations. A physiologically tolerated buffer is preferably added to provide improved pH control. The formulations can cover a wide range of pHs, such as from about pH 4 to about pH 10, and preferred ranges from about pH 5 to about pH 9, and a most preferred range of about 6.0 to about 8.0. Preferably the formulations of the present invention have pH between about 6.8 and about 7.8. Preferred buffers include phosphate buffers, most preferably sodium phosphate, particularly phosphate buffered saline (PBS).

Other additives, such as a pharmaceutically acceptable solubilizers like Tween 20 (polyoxyethylene (20) sorbitan monolaurate), Tween 40 (polyoxyethylene (20) sorbitan monopalmitate), Tween 80 (polyoxyethylene (20) sorbitan monooleate), Pluronic F68 (polyoxyethylene polyoxypropylene block copolymers), and PEG (polyethylene glycol) or non-ionic surfactants, such as polysorbate 20 or 80 or poloxamer 184 or 188, Pluronic™ polyls, other block co-polymers, and chelators such as EDTA and EGTA can optionally be added to the formulations or compositions to reduce aggregation. These additives are particularly useful if a pump or plastic container is used to administer the formulation. The presence of pharmaceutically acceptable surfactant mitigates the propensity for the protein to aggregate.

The formulations of the present invention can be prepared by a process which comprises mixing at least one anti-CNGH0010 antibody and a preservative selected from the group consisting of phenol, m-cresol, p-cresol, o-cresol, chlorocresol, benzyl alcohol, alkylparaben, (methyl, ethyl, propyl, butyl and the like), benzalkonium chloride, benzethonium chloride, sodium dehydroacetate and thimerosal or mixtures thereof in an aqueous diluent. Mixing the at least one anti-CNGH0010 antibody and preservative in an aqueous diluent is carried out using conventional dissolution and mixing procedures. To prepare a suitable formulation, for example, a measured amount of at least one anti-CNGH0010 antibody in buffered solution is combined with the desired preservative in a buffered solution in quantities sufficient to provide the protein and preservative at the desired concentrations. Variations of this process would be recognized by one of ordinary skill in the art. For example, the order the components are added, whether additional additives are used, the temperature and pH at which the formulation is prepared, are all factors that can be optimized for the concentration and means of administration used.

The claimed formulations can be provided to patients as clear solutions or as dual vials comprising a vial of lyophilized, at least one anti-CNGH0010 antibody that is reconstituted with a second vial containing water, a preservative and/or excipients, preferably, a phosphate buffer and/or saline and a chosen salt, in an aqueous diluent. Either a single solution vial or dual vial requiring reconstitution can be reused multiple times and can suffice for a single or multiple cycles of patient treatment and thus can provide a more convenient treatment regimen than currently available.

The present claimed articles of manufacture are useful for administration over a period of immediately to twenty-four hours or greater. Accordingly, the presently claimed articles of manufacture offer significant advantages to the patient. Formulations of the invention can optionally be safely stored at temperatures of from about 2 to about 40° C. and retain the biologically activity of the protein for extended periods of time, thus, allowing a package label indicating that the solution can be held and/or used over a period of 6, 12, 18, 24, 36, 48, 72, or 96 hours or greater. If preserved diluent is used, such label can include use up to 1-12 months, one-half, one and a half, and/or two years.

The solutions of at least one anti-CNGH0010 antibody in the invention can be prepared by a process that comprises mixing at least one antibody in an aqueous diluent. Mixing is carried out using conventional dissolution and mixing procedures. To prepare a suitable diluent, for example, a measured amount of at least one antibody in water or buffer is combined in quantities sufficient to provide the protein and, optionally, a preservative or buffer at the desired concentrations. Variations of this process would be recognized by one of ordinary skill in the art. For example, the order the components are added, whether additional additives are used, the temperature and pH at which the formulation is prepared, are all factors that can be optimized for the concentration and means of administration used.

The claimed products can be provided to patients as clear solutions or as dual vials comprising a vial of lyophilized (at least one) anti-CNGH0010 antibody that is reconstituted with a second vial containing the aqueous diluent. Either a single solution vial or dual vial requiring reconstitution can be reused multiple times and can suffice for a single or multiple cycles of patient treatment and thus provides a more convenient treatment regimen than currently available.

The claimed products can be provided indirectly to patients by providing to pharmacies, clinics, or other such institutions and facilities, clear solutions or dual vials comprising a vial of lyophilized (at least one) anti-CNGH0010 antibody that is reconstituted with a second vial containing the aqueous diluent. The clear solution in this case can be up to one liter or even larger in size, providing a large reservoir from which smaller portions of the at least one antibody solution can be retrieved one or multiple times for transfer into smaller vials and provided by the pharmacy or clinic to their customers and/or patients.

Recognized devices comprising these single vial systems include those pen-injector devices for delivery of a solution such as BD Pens, BD Autojector®, Humaject®, NovoPen®, B-D®Pen, AutoPen®, and OptiPen®, GenotropinPen®, Genotronorm Pen®, Humatro Pen®, Reco-Pen®, Roferon Pen®, Biojector®, Iject®, J-tip Needle-Free Injector®, Intraject®, Medi-Ject®, e.g., as made or developed by Becton Dickensen (Franklin Lakes, N.J., www.bectondickenson.com), Disetronic (Burgdorf, Switzerland, www.disetronic.com; Bioject, Portland, Oreg. (www.bioject.com); National Medical Products, Weston Medical (Peterborough, UK, www.weston-medical.com), Medi-Ject Corp (Minneapolis, Minn., www.mediject.com). Recognized devices comprising a dual vial system include those pen-injector systems for reconstituting a lyophilized drug in a cartridge for delivery of the reconstituted solution such as the HumatroPen®.

The products presently claimed include packaging material. The packaging material provides, in addition to the information required by the regulatory agencies, the conditions under which the product can be used. The packaging material of the present invention provides instructions to the patient to reconstitute the (at least one) anti-CNGH0010 antibody in the aqueous diluent to form a solution and to use the solution over a period of 2-24 hours or greater for the two vial, wet/dry, product. For the single vial, solution product, the label indicates that such solution can be used over a period of 2-24 hours or greater. The presently claimed products are useful for human pharmaceutical product use.

The formulations of the present invention can be prepared by a process that comprises mixing at least one anti-CNGH0010 antibody and a selected buffer, preferably, a phosphate buffer containing saline or a chosen salt. Mixing the (at least one) anti-CNGH0010 antibody and buffer in an aqueous diluent is carried out using conventional dissolution and mixing procedures. To prepare a suitable formulation, for example, a measured amount of at least one antibody in water or buffer is combined with the desired buffering agent in water in quantities sufficient to provide the protein and buffer at the desired concentrations. Variations of this process would be recognized by one of ordinary skill in the art. For example, the order the components are added, whether additional additives are used, the temperature and pH at which the formulation is prepared, are all factors that can be optimized for the concentration and means of administration used.

The claimed stable or preserved formulations can be provided to patients as clear solutions or as dual vials comprising a vial of lyophilized (at least one) anti-CNGH0010 antibody that is reconstituted with a second vial containing a preservative or buffer and excipients in an aqueous diluent. Either a single solution vial or dual vial requiring reconstitution can be reused multiple times and can suffice for a single or multiple cycles of patient treatment and thus provides a more convenient treatment regimen than currently available.

Other formulations or methods of stablizing the anti-CNGH0010 antibody may result in other than a clear solution of lyophilized powder comprising the antibody. Among non-clear solutions are formulations comprising particulate suspensions, the particulates being a composition containing the anti-CNGH0010 antibody in a structure of variable dimension and known variously as a microsphere, microparticle, nanoparticle, nanosphere, or liposome. Such relatively homogenous essentially spherical particulate formulations containing an active agent can be formed by contacting an aqueous phase containing the active and a polymer and a nonaqueous phase followed by evaporation of the nonaqueous phase to cause the coalescence of particles from the aqueous phase as taught in U.S. Pat. No. 4,589,330. Porous microparticles can be prepared using a first phase containing active and a polymer dispersed in a continuous solvent and removing the solvent from the suspension by freeze-drying or dilution-extraction-precipitation as taught in U.S. Pat. No. 4,818,542. Preferred polymers for such preparations are natural or synthetic copolymers or polymer selected from the group consisting of gleatin agar, starch, arabinogalactan, albumin, collagen, polyglycolic acid, polylactic aced, glycolide-L(−) lactide poly(episilon-caprolactone, poly(epsilon-caprolactone-CO-lactic acid), poly(epsilon-caprolactone-CO-glycolic acid), poly(B-hydroxy butyric acid), polyethylene oxide, polyethylene, poly(alkyl-2-cyanoacrylate), poly(hydroxyethyl methacrylate), polyamides, poly(amino acids), poly(2-hydroxyethyl DL-aspartamide), poly(ester urea), poly(L-phenylalanine/ethylene glyco 1,6-diisocyanatohexane) and poly(methyl methacrylate). Particularly preferred polymers are polyesters, such as polyglycolic acid, polylactic aced, glycolide-L(−) lactide poly(episilon-caprolactone, poly(epsilon-caprolactone-CO-lactic acid), and poly(epsilon-caprolactone-CO-glycolic acid. Solvents useful for dissolving the polymer and/or the active include: water, hexafluoroisopropanol, methylenechloride, tetrahydrofuran, hexane, benzene, or hexafluoroacetone sesquihydrate. The process of dispersing the active containing phase with a second phase may include pressure forcing the first phase through an orifice in a nozzle to effect droplet formation.

Dry powder formulations may result from processes other than lyophilization, such as by spray drying or solvent extraction by evaporation or by precipitation of a crystalline composition followed by one or more steps to remove aqueous or nonaqueous solvent. Preparation of a spray-dried antibody preparation is taught in U.S. Pat. No. 6,019,968. The antibody-based dry powder compositions may be produced by spray drying solutions or slurries of the antibody and, optionally, excipients, in a solvent under conditions to provide a respirable dry powder. Solvents may include polar compounds, such as water and ethanol, which may be readily dried. Antibody stability may be enhanced by performing the spray drying procedures in the absence of oxygen, such as under a nitrogen blanket or by using nitrogen as the drying gas. Another relatively dry formulation is a dispersion of a plurality of perforated microstructures dispersed in a suspension medium that typically comprises a hydrofluoroalkane propellant as taught in WO 99/16419. The stabilized dispersions may be administered to the lung of a patient using a metered dose inhaler. Equipment useful in the commercial manufacture of spray dried medicaments are manufactured by Buchi Ltd. or Niro Corp.

At least one anti-CNGH0010 antibody in either the stable or preserved formulations or solutions described herein, can be administered to a patient in accordance with the present invention via a variety of delivery methods including SC or IM injection; transdermal, pulmonary, transmucosal, implant, osmotic pump, cartridge, micro pump, or other means appreciated by the skilled artisan, as well-known in the art.

EXAMPLES OF INVENTION

Having generally described the invention, the same will be more readily understood by reference to the following examples, which are provided by way of illustration and are not intended as limiting.

It will be clear that the invention can be practiced otherwise than as particularly described in the foregoing description and examples.

Numerous modifications and variations of the present invention are possible in light of the above teachings and, therefore, are within the scope of the appended claims.

Example 1 CNGH0010 Sequence Data

The CNGH0010 genomic nucleotide sequence (SEQ ID NO:1) spans 16356 bp. Based on modeling with several gene prediction algorithms, such as GeneScan, Fgenesh (http://genome.ucsc.edu/) and the Acembly program (http://www.acedb.org/Cornell/acembly/), CNGH0010 is predicted to comprise 25 exons (FIG. 1, Table 1). Exons 1, 7 and 18 each contain a start codon and are downstream from promoter, enhancer, and other regulatory motifs; these exons may be utilized as initiation exons. Exons 15 and 23 contain a stop codon and can be utilized as termination exons. Five categories of alternatively spliced transcripts have been identified and are exemplified in CNGH0010.1, CNGH0010.2, CNGH0010.3, CNGH0010.4, and CNGH0010.5 (SEQ ID NOS: 2, 4, 6, 8, and 10, respectively, Table 2).

TABLE 1 CNGH0010 exon composition and description start stop Exon # position position # of bp frame Note  1 101 526 426 In 1^(st) ini. Exon; Constant for 10.1 and 10.2  2 786 986 201 In Constant for 10.1 and 10.2  3 1099 1155 57 In Constant for 10.1 and 10.2  4 1763 1813 51 In Constant for 10.1 and 10.2  5 1983 2165 183 In Constant for 10.1 and 10.2  5a 1983 2076 85 out left exon  5b 2117 2165 91 out right exon  6 2936 2980 45 In rare exon  7 3149 3205 57 In 2^(nd) initiation exon; Constant for 10.3 and 10.4  7a 3168 3197 30 out  8 3324 3392 69 In Constant for 10.3 and 10.4  8a 3189 3392 204 out overlap with exon 8 but longer  9 3615 3665 51 In Alternatively spliced 10 5336 5371 36 In Alternatively spliced 11 6065 6118 54 In Alternatively spliced 12 7391 7450 60 In Alternatively spliced 13 7590 7637 48 In Constant for 10.1, 10.2, 10.3, and 10.4 14 7811 7858 48 In Constant for 10.1, 10.2, 10.3, and 10.4 15 10129 10155 27 In 1^(st) term. Exon 16 10690 10746 57 In Constant for 10.1, 10.2, 10.3, and 10.4 17 11393 11440 48 In Constant for 10.1, 10.2, 10.3, and 10.4 18 11679 11753 75 In 3^(rd) initiation exon, constant for 10.5 19 12996 13043 48 In Constant for 10.1, 10.3 and 10.5 20 13157 13198 42 In Alternatively spliced 21 13547 13618 72 In Constant for 10.1, 10.3 and 10.5 22 14679 14702 24 In Constant for 10.1, 10.3 and 10.5 23 14813 14860 48 In Constant for 10.1, 10.3 and 10.5 24 15895 15929 35 NA 3′UTR-1 25 16038 16356 319 NA 3′UTR-2

Table 2 shows the various CNGH0010 transcripts and exons contained within each transcript. The exons shown in bold are constant in each transcript, while the other exons listed for each transcript are alternatively spliced and, optionally, part of various transcripts. As shown in Table 2, the nucleotide and amino acid sequences for each transcript vary depending on the exact combination of exons present.

TABLE 2 CNGH0010 transcripts description Nucleotide Length Peptide Transcript Exons (bp) Length (aa) CNGH0010.1 1, 2, 3, 4, 5, 6, 8, 9, 10, 11, 1809/2132 459/555 12, 13, 14, 16, 17, 19, 20, 21, 22, 23, 24, 25 CNGH0010.2 1, 2, 3, 4, 5, 8, 9, 10, 11, 12, 1533/1734 373/440 13, 14, 15 CNGH0010.3 7, 8, 9, 10, 11, 12, 13,  881/1159 172/253 14, 16, 17, 19, 20, 21, 22, 23, 24, 25 CNGH0010.4 7, 8, 9, 10, 11, 12, 13, 14, 15 445/646  82/149 CNGH0010.5 18, 19, 21, 22, 23, 25 600 88

CNGH0010.1 is any transcript that starts with exon 1 and ends at exon 25, excluding exons 7, 15, and 18. It may have as as few as 15 exons (i.e., exons 1-5, 8, 13, 14, 16, 17, 19, 21-23, and 25) or as many as 22 exons (i.e., exons 1-6, 8-14, 16, 17, and 19-25). Exons 6, 9-12, 20, and 24 can be differentially spliced, either individually or in any combination. Therefore, CNGH0010.1 transcripts range from 1809 to 2132 bp. They encode peptides ranging from 459 to 555 amino acids, depending on the exon composition.

CNGH0010.2 is any transcript that starts with exon 1 and ends at exon 15, excluding exons 6 and 7. It may have as few as 9 exons (i.e., exons 1-5, 8, and 13-15) or as many as 13 exons (i.e., exons 1-5 and 8-15). Exons 9-12 can be differentially spliced, either individually or in any combination. Therefore, CNGH0010.2 transcripts range from 1533 to 1734 bp, encoding peptides ranging from 373 to 440 amino acids, depending on the exon composition.

CNGH0010.3 is any transcript that starts with exon 7 and ends at exon 25, excluding exons 15 and 18. It may have as few as 11 exons (i.e., exons 7, 8, 13, 14, 16, 17, 19, 21-23, and 25) or as many as 17 exons (i.e., exons 7-14, 16, 17, and 19-25). Exons 9-12, 20, and 24 can be differentially spliced, either individually or in any combination. Therefore, CNGH0010.3 transcripts range from 881 to 1159 bp, encoding peptides ranging from 172 to 253 amino acids, depending on the exon composition.

CNGH0010.4 is any transcript that starts with exon 7 and ends at exon 15. It may have as few as 5 exons (i.e., exons 7, 8, and 13-15) or as many as 9 exons (i.e., exons 7-15). Exons 9-12 can be differentially spliced, either individually or in any combination. Therefore, CNGH0010.4 transcripts range from 445 to 646 bp, encoding peptides ranging from 82 to 149 amino acids, depending on the exon composition.

CNGH0010.5 is any transcript that starts with exon 18 and ends at exon 25, excluding exons 20 and 24. It has 6 exons, i.e., exons 18, 19, 21-23, and 25. The CNGH0010.5 transcript contains 600 bp encoding a peptide of 88 amino acids.

In addition to these 5 categories, a transcript that contains exons 5a, 5b, 7a, or 8a will have out-of-frame splicing at the site where these exons begin in the corresponding transcripts; this may result in truncated proteins at the site of the exon or downstream of the exon. Often, the truncated proteins use an alternative initiation ATG codon in exon 13, at nucleotide position 7611.

The CNGH0010.1 amino acid sequence of SEQ ID NO:3 has 94% identity over 449 residues to GenBank Accession No. AY358412 (Pat. Publ. No. WO/200061623); the CNGH0010.2 amino acid sequence of SEQ ID NO:5 has 100% identity over 440 residues to Dgen No. AAF54238 (Pat. Publ. No. WO/200078961); the CNGH0010.3 amino acid sequence of SEQ ID NO:7 has 99% identity over 127 residues to Dgen No. AAH23810 (Pat. Publ. No. WO/200132888); the CNGH0010.4 amino acid sequence of SEQ ID NO:9 has 98% identity over 93 residues to Dgen No. ADE28278 (Pat. Publ. No. WO/2003046152); and the CNGH0010.5 amino acid sequence of SEQ ID NO: 11 has 85% identity over 102 residues to Dgen No. AAF97894 (Pat. Publ. No WO/200121658).

Example 2 CNGH0010 Transcripts

5′ and 3′-RACE (Rapid Analysis of cDNA Ends) was performed on total RNA from A431 cells and normal adult human male skin tissue according to the manufacturer's protocol (Catalog number L1502-01, Invitrogen, Corp., Carlsbad, Calif.). Briefly, 5 μg of total RNA was dephosphorylated with calf intestine alkaline phosphatase to remove phospho-groups from non-mRNA or truncated mRNA. The RNA was then treated with Tobacco Acid Pyrophosphatase to remove the 5′ cap structure from mature mRNA. An RNA oligonucleotide of known sequence was then ligated to the 5′ ends of mature mRNA, and then used as a template for reverse transcription with Superscript RT enzyme, primed with an oligo dT primer that also contained a unique known sequence. RT was carried out at 42° C. for 1.5 hours. The resulting cDNAs contained common sequences at their 5′ ends and 3′ ends, and could be used with nested oligonucleotides specific for the CNGH0010 gene (SEQ ID NOS: 12-21, Table 3) to amplify all or part of the cDNA through PCR.

TABLE 3 RACE primers SEQ ID NO: Olligo name Sequence and exon 12 CNGH0010EX1F GGC TGG GCA GAG ATG AAG TTC CAG EXON1 13 CNGH0010EX1FNEST TCT GCC TGG GCA GTG GGG AG EXON1 14 CNGH0010EX7F ATG CTC GGA ATA ACT TCC TGC AGC G EXON7 15 CNGH0010EX7FNEST GCA GCG ACC AAC AGG CTA AAG EXON7 16 CNGH0010EX18F ATG AAG CCG GCC ACT GCC TCTG EXON18 17 CNGH0010EX18FNEST CTC TGC TCC TGC TCC TGC TG EXON18 18 CNGH0010UTR2R GGG CCA GGG CTG GCA CAG GC UTR2 19 CNGH0010UTR2NEST CGG GGC CTC GGT GGT GGT TGC UTR2 20 CNGH0010EX15R TCT GGT GGC TCC TTG TCT GGA GGT C EXON15 21 CNGH0010EX15RNEST GTC ACG GGA TGC GAG AGC TTC TCT GGT C EXON15

SEQ ID NOS:12 or 13 in exon 1 with SEQ ID NOS:18 or 19 in exon 25 (3′UTR-2) were used to amplify CNGH0010.1 transcripts. SEQ ID NOS:12 or 13 with SEQ ID NOS:20 or 21 in exon 15 were used to amplify CNGH0010.2 transcripts. SEQ ID NOS:14 or 15 in exon 7 with SEQ ID NOS:18 or 19 in exon 25 were used to amplify CNGH0010.3 transcripts. SEQ ID NOS:14 or 15 in exon 7 with SEQ ID NOS:20 or 21 in exon 15 were used to amplify CNGH0010.4 transcripts. SEQ ID NOS:16 or 17 in exon 18 with SEQ ID NOS:18 or 19 in exon 25 were used to amplify CNGH0010.5 transcripts. RT-PCR data, as shown in FIG. 2, demonstrated that the transcripts of CNGH0010.1 (SEQ ID NO:2), 10.2 (SEQ ID NO:4) are at the highest level, followed by 10.5 (SEQ ID NO:10) at a lower level, 10.4 (SEQ ID NO:8) at a significantly lower level, and 10.3 (SEQ ID NO:6) at the lowest level of all of the transcripts.

As shown in Table 4 below, five sets of forward/reverse primers and probes were designed to identify the five dominant splice variants by real time PCR application. For each splice variant, the forward and reverse primers and Taqman probe are shown. Total RNA extracted from A431 and HCT116 cells treated with various concentrations of TNFα, LPS, and IL-12 was reversed transcribed into a cDNA template, which was then amplified by real time PCR using these 5 sets of primers/probes. CNGH0010.2 and CNGH0010.5 were upregulated by various concentrations of TNFα, LPS, and IL-12.

TABLE 4 Forward/reverse primers and probes of real time PCR for splice variants Splice variant Forward primer Reverse primer Taqman Probe CNGH0010.1 SEQ ID NO:25: SEQ ID NO:26: SEQ ID NO:27: GAGGTGACAGCG TTAAAATTCTTCCAGA ATTCAGAACTCTGA GCAGTGAGT AAGTGTCAAAGTTA GACGTC CNGH0010.2 SEQ ID NO:28: SEQ ID NO:29: SEQ ID NO:30: TGTTGGTGGAGTC CGGGATGCGAGAGCTT CACTTTCTGGAAGA AATACTGTGAACT CTC ATTTTAAATC CNGH0010.3 SEQ ID NO:31: SEQ ID NO:32: SEQ ID NO:33: GGAGCGGCGGAG TGATGAAACCCAGCTT AAACCCGGGAACT GAAAT GGATT CTGAGAC CNGH0010.4 SEQ ID NO:34: SEQ ID NO:35: SEQ ID NO:36: GGCGGAGGAAAT GAGCTTCTCTGGTCCTT AATCTGGGATTCAG GGACATAAA GTTTATGG AACTC CNGH0010.5 SEQ ID NO:37: SEQ ID NO:38: SEQ ID NO:39: GGGTGCGGACGC GTCTTGACTGAGTACT ACGATCAGAACTA GTCAT TCCCACCATAG CAATTACAAC

Example 3 Predicted CNGH0010 Protein Domains

The CNGH0010.1 and CNGH0010.2 polypeptides may contain up to 555 and 440 amino acids, respectively (SEQ ID NOS:3 and 5, respectively). The first 21 amino acids encode a signal peptide, followed by five major domains (FIG. 3). The first domain, which includes the signal peptide, is encoded by exon 1, and has no significant homology to any known proteins or protein domains. This domain is predicted to form at least 6 subdomains of alpha-helical secondary structure based on the NNPredict program. The second domain, encoded by exon 2, posseses 19 Glycine-X-Y repeats that are known to form coiled-coiled structures, as seen in collagen and collagen-like molecules. This domain is then followed by a differentially spliced serine-glycine rich domain (up to 42% serine, 37% glycine), encoded by exons 4-8. The differential splicing appears to alter the size and amount of serine-glycine residues.

A differentially spliced spacer domain is encoded by exons 9-17. The exons encoding this region are very small, ranging in size from 36 to 60 nucleotides. This region is predicted to have minimal if any secondary structure using the NNPredict program. The differential splicing that occurs in this region appears to regulate the distance between the serine-glycine rich domain, and the C-terminal domain. The CNGH0010.1 (SEQ ID NO:3) terminates in another domain encoded by exons 19-23 that has no homology to any known proteins. This domain is predicted to have at least 2 regions of predicted alpha-helix. The CNGH0010.2 (SEQ ID NO:5) polypeptide posseses all of the domains included in the 10.1 (SEQ ID NO:3) polypeptide, except for the C-terminal domain encoded by exons 19-23. The CNGH0010.3 (SEQ ID NO:7) polypeptide may contain up to 253 amino acids and contains part of the differentially spliced Serine-Glycine rich domain, the differentially spliced spacer domain, and the C-terminal domain. The CNGH0010.4 (SEQ ID NO:9) polypeptide may contain up to 149 and includes part of the differentially spliced Serine-Glycine rich domain and the differentially spliced spacer domain. Finally, the CNGH0010.5 (SEQ ID NO:11) polypeptide has 88 amino acids and contains essentially the C-terminal domain, preceeded by a signal peptide encoded by exon 18.

The domains of CNGH0010 allow for the assembly of a homo (all CNGH0010.1 (SEQ ID NO:3)) or all CNGH0010.2 (SEQ ID NO:5)) or hetero (mixture of CNGH0010.1 (SEQ ID NO:3) and CNGH0010.2 (SEQ ID NO:5))-trimers, such as collagens or adiponectin, through the collagen-like coiled-coil region. The presence of proline residues at some of the X-Y positions of the Gly-X-Y repeat is thought to stabilize these trimers, by unknown mechanisms and thus provides further evidence that the molecule might form collagen-like structures. Preliminary biochemical characterization of recombinantly expressed CNGH0010.2 (SEQ ID NO:5) polypeptide indicates that this molecule does indeed form oligomers. SDS-PAGE analysis (as shown in FIG. 4) indicates that molecules with molecular weights of 2, 3 and 4 times that of the single chain exist in both non-reduced and reduced samples, indicating that some of the oligomers are covalently bound. This result has been confirmed by SELDI mass spectrometry and gel filtration HPLC. As seen in collagen molecules, covalent cross-linking between trimer chains can be seen by post-translational modification of Lysine residues present in the polypeptide. This modification results in covalent dimer, trimer, and multimers (fibrils) of the polypeptide. The CNGH0010.5 (SEQ ID NO:11) molecules are essentially the C-terminal domain and may have unique functional activity.

Example 4 Secretion of CNGH0010 Polypeptides

The CNGH0010.1 and 10.2 polypeptides contain the same predicted signal sequence (amino acids 1-21 in SEQ ID NOS:3 and 5). The predicted CNGH0010.5 polypeptide sequence has a different signal sequence (amino acids 1-24 in SEQ ID NO: 11). In vitro transient expression of a His tagged CNGH0010.2 fusion protein, as well as a CNGH0010.5 mimetibody (the details of which are described in Example 6), confirmed that the signal sequences indeed target these polypeptides for extracellular secretion. Therefore, CNGH0010.1 (SEQ ID NO:3), 10.2 (SEQ ID NO:5), and 10.5 (SEQ ID NO:11) polypeptides probably are secreted into the extracellular space where they might exert their effects. CNGH0010.3 and CNGH0010.4 (SEQ ID NOS:7 and 9) do not contain a signal sequence.

Example 5 Relative CNGH0010 Transcript Levels in Selected Disease Tissues

CNGH0010 primers and probes, Primers: CNGH00010as1-GGC GGA GGA AAT GGA CAT AA (SEQ ID NO:23), CNGH00010s1-GCT TGG ATT TAA AAT TCT TCC AGA AA (SEQ ID NO:24), TaqMan MGB Probe: CNGH00010p1-6FAM-GCT TTT CAC ACC CGG GT-MGBNFQ (SEQ ID NO:22) were designed using Primer Express software and synthesized by Applied Biosystem (Foster City, Calif.). Total RNAs were isolated from different tissues, reverse transcribed and amplified by PCR using these primers/probes. Relative transcript levels of CNGH0010 are shown below in Table 5.

TABLE 5 Distribution of CNGH0010 in different human disease tissues Fold Tissues Disease change* Brain Normal 1.00 Lung Emphysema 4.58 Lung respiratory infection 0.19 Tonsil Tonsillitis 1.63 Thyroid grave's disease 8.35 Thyroid lymphocytic thyroidities 3.90 Pancreas Diabetes 9.45 Pancreas Pancreatitis 0.86 Liver Cirrhosis 0.45 Colon Colitis 0.24 Colon UC 0.22 Synovium osteoarthritis/DJD 0.14 Catilage osteoarthritis/DJD 1.32 Ovary endometriosis 2.18 Bladder cystitis 0.19 Lymphoma hodgkin 0.06 Sarcoma 0.21 *The level of CNGH0010 in each tissue is compared to the level in normal brain tissue that acts as the control (1.00 Fold Change).

When compared with calibration tissue, normal human brain RNA, an increase in CNGH0010 mRNA level was detected in emphysematous lung tissue, thyroid tissue from Grave's disease patient or inflammatory thyroiditis, inflamed tonsil, ovary from endometriosis patient, diabetic pancreas and osteoarthritic cartilage.

Example 6 Protein Expression

Expression of the CNGH0010.2 (SEQ ID NO:5) protein was performed by cloning most of a CNGH0010.2 transcript containing exons 1-5, 8, 9, 12 and part of 13 inframe of a hexa-His tag in an expression vector driven by a CMV promoter. This construct was transfected into HEK293 cells and purified with the His tag. The N-terminal sequence of the expressed and purified material confirmed the identity of the purified protein and demonstrated signal peptide cleavage. SDS-PAGE analysis of the expressed and purified protein indicated that the molecule forms oligomers (FIG. 4), which was confirmed by non-reducing MS-SELDI (surface enhanced laser desorption/ionization) and gel filtration HPLC. This data indicates that the CNGH0010.2 and CNGH0010.1 transcripts, since they contain the same signal sequence encoded by exon 1, have the ability to be secreted extracellularly. In addition, the SDS-PAGE, SELDI-MS, and gel filtration HPLC indicate that this molecule has the ability to form oligomers.

CNGH0010.5 (SEQ ID NO:11) could not be expressed alone in HEK293 cells; however, it was engineered as a mimetibody. Most of the CNGH0010.5 coding region containing amino acids 1 to 86 were engineered into an expression plasmid that contained the human IgH J2 segment fused to the human IgG1 hinge, CH₂ and CH₃. The plasmid contained a CMV promoter for transcription of recombinant genes, and utilized the CNGH0010.5 endogenous signal sequence encoding amino acids 1-24. This construct was transiently transfected into HEK293 cells, and the resulting secreted molecules purified by protein A affinity beads. SDS-PAGE analysis confirmed that a protein of predicted molecular weight containing the CNGH0010.5 mature amino acid sequence, followed by the J2, hinge, CH₂ and CH₃ of the human IgG1 had been expressed.

The expression levels of the CNGH0010.2 (SEQ ID NO:5) and CNGH0010.5 (SEQ ID NO:11) proteins in A431 and HCT116 cells were measured in response to stimulation by TNF-α and LPS. Stimulation by TNF-α and LPS caused an increase in CNGH0010.2 (SEQ ID NO:5) and CNGH0010.5 (SEQ ID NO:11) expression. Similarly, expression of CNGH0010.2 (SEQ ID NO:5) and CNGH0010.5 (SEQ ID NO:11) was increased in the presence of IL-12. Additionally, IL-6, IL-8, and GMCSF levels were increased by TNF-α treatment in A431 cells and they were reduced in the presence of a chimeric, anti-TNF-α antibody. IL-6 is an important inflammatory cytokine, the increase of this cytokine accompanied by the increase of CNGH0010.2 and 10.5 with TNF-α treatment indicates a possible mechanism of CNGH0010 and inflammatory responses. IL-8 is a chemokine that plays a critical role in inflammation. It recruits lymphocytes and leukocytes to the inflammatory site and stimulates other cytokine production. GMCSF is a stimulator for macrophage/monocytes as well as other lymphocytes, which also play roles in the inflammatory responses. This evidence suggests that CNGH0010 may play a role in the inflammatory regulation, therefore it could be a good target for therapeutic development.

Example 7 Protein Analysis

cDNAs for CNGH0010.1, 10.2, a truncated 10.2 (exons 1-5, 8, 9, 12, and 13) (SEQ ID NO:40), and 10.5 were cloned into commercial vector pcDNA3. Imychis using novel restriction sites present in the vector and cDNA. These expression plasmids were sequenced, and then transfected into HEK293H cells using Lipofectamine 2000. Using a carboxyl terminal 6× Histidine tag, recombinantly expressed protein was purified on a Talon resin.

Recombinantly expressed proteins were analyzed by SDS-PAGE, anti-myc western blot, MALDI-MS, and SEC HPLC. In addition, O-linked glycosylation was analyzed by first treating the proteins with O-glycosidase with and without sialidase. The released O-glycans were labeled with anthranilic acid and analyzed by HPLC. The truncated CNGH0010.2 protein containing exons 1-5, 8, 9, 12, and 13 (SEQ ID NO:41) is predicted to be 37.5 kDa. However, SDS-PAGE analysis clearly shows this molecule running at an apparent molecular weight of 45 kDa. In addition, it appears as if the molecule has a propensity to multimerize, as non-reduced analysis by SDS-PAGE, SELDI-MS (FIG. 5), and SEC-HPLC (FIG. 6), all indicate that dimeric and trimeric forms of the truncated CNGH0010.2 molecule exist in solution.

The apparent descrepency between the predicted MW and the observed by SDS-PAGE, might be explained by the presence of O-linked oligosaccharides covalently attached to the molecule. Glycosylation analysis of this protein clearly indicates the presence of such moieties (FIG. 7). The function of such groups on molecules is not completely understood. It has been speculated that they may aid in solubility, or delineate a region that is resistant to protease cleavage.

SDS-PAGE analysis of recombinantly expressed and tagged CNGH0010.1, CNGH0010.2, and CNGH0010.5 similarly showed discrepancies between predicted and apparent molecular weight (data not shown). Interestingly, all four proteins have stretches of serine and/or threonine residues that could serve as O-linked glycosylation sites that might be modified. This would account for the differences in the predicted and actual molecular weight migration on SDS-PAGE. The CNGH0010.1 and CNGH0010.2 variants possess identical stretches to those in the truncated CNGH0010.2 (SEQ ID NO:41) that has been confirmed to contain such glycosylation sites, and therefore, likely do as well.

Example 8 Antibody Generation Rabbit Anti-CNGH0010.5 Polyclonal Antibody Generation

Recombinantly expressed CNGH0010 protein (exons 1-5, 8, 9, 12, and 13) or chemically synthesized CNGH0010.5 was used to immunize New Zealand White rabbits on weeks 0, 2, 7, and 8. After 10 weeks, CNGH0010 specific antibodies were affinity purified using the recombinant CNGH0010 or chemically synthesized CNGH0010.5. These antibodies were tested for specificity by western blot analysis, with recombinant CNGH0010 isoforms as the target.

Mouse Anti-CNGH0010 Monoclonal Antibody Generation

Three Balb/c mice (Charles River Laboratories) were immunized intraperitoneally (IP) with 1 nanomole of prostaglandin E2 (PGE2) (Sigma) on day 1, then 3 hours later, received a second IP injection with 50 μg of human recombinant CNGH0010.2 truncated protein (SEQ ID NO:41) emulsified in Titermax adjuvant (Sigma). On days 2 and 3, the mice received additional IP injections of PGE2 and were then subsequently boosted with 50 μg truncated CNGH0010.2 in Titermax on days 21, 42, and 100. The mice were bled at various time points throughout the immunization schedule.

A cell bank of the non-secreting Balb/c mouse myeloma fusion partner, FO, was purchased from ATCC (# CRL-1646). One frozen vial of FO cells was received, thawed and resuspended in αMEM (modified) medium (JRH Biosciences) supplemented with 10% (v/v) FBS (Cell Culture Labs), 1 mM sodium pyruvate, 0.1 mM NEAA, 2 mM L-glutamine (all from JRH Biosciences). The cells were expanded, cryopreserved in 95% FBS and 5% DMSO (Sigma) and stored in a vapor phase liquid nitrogen freezer in CBS. The cell bank was sterile (internal Quality Control) and free of mycoplasma (tested by Bionique Laboratories). This cell line was thawed and maintained in log phase growth in the media described above for several days prior to fusion. The cells were washed in αMEM, counted, and viability determined (>85%) by Guava Viacount prior to fusion.

Six days prior to fusion, the mice were boosted IP with 50 μg of truncated CNGH0010.2 diluted in 200 μl PBS and three days prior to fusion, the mice were boosted with 100 μg anti-CD40 agonist Mab (R&D Systems). On fusion day, the mice were sacrificed by cervical dislocation and the spleens were removed aseptically and immersed in 10 mL of cold phosphate-buffered saline (PBS) containing 100 U/mL penicillin, 0.1 mg/mL streptomycin, and 0.25 μg/mL amphotericin B (PSA) (Sigma). The splenocytes were harvested by grinding through a fine mesh screen with a small pestle and rinsing with warm αMEM. The cells were washed and diluted to 2×10⁷ cells/mL. The cells were then layered onto Lymphocyte-M density separation medium (Accurate) and centrifuged at 1200×g for 20 minutes at RT. PBMC at the interface were removed and washed once more in warm αMEM. Fusions were carried out at a 1:1 ratio of FO murine myeloma cells to viable spleen cells according to the method of De St. Groth. Briefly, spleen and myeloma cells were mixed together, pelleted and washed twice in 50 mL of αMEM supplemented with 2 mM L-glutamine (JRH Biosciences) and 25 μg/mL gentamicin (Sigma). The pellet was resuspended with 1-2 mL of polyethylene glycol (PEG) solution (2 g PEG molecular weight 4000, 2 mL αMEM, 0.4 mL DMSO) at 37° C. over 1 minute. The cell/fusion mixture was then immersed in a 37° C. water bath for approximately 60 seconds with gentle agitation. The fusion reaction was stopped by adding 37° C. αMEM: 1 mL in the first minute, 15 mL in the next 3 minutes, and approximately 33 mL in the following minute. The fused cells were allowed to rest for 5 minutes at RT and then centrifuged at 150×g for 5 minutes. The cells were resuspended in HAT medium (αMEM (modified), supplemented with 20% FBS, 5% Origen, 1 mM sodium pyruvate, 0.1 mM NEAA, 2 mM L-glutamine, 25 μg/mL gentamicin (Sigma) and HAT (100 μM hypoxanthine, 0.4 μM aminopterin, and 16 μM thymidine—Sigma)) and then seeded in 96-well flat bottom polystyrene tissue culture plates (Corning # 25860). The fusion plates were then placed in a humidified 37° C. incubator containing 7% CO₂ and left undisturbed for 7-10 days.

Solid phase EIA was used to screen mouse sera for titers and hybridoma supernatants for antibodies specific for human CNGH0010. Briefly, plates (Nunc-Maxisorp #446612) were coated overnight with human CNGH0010 at 2 μg/mL in PBS. After washing in 0.15 M saline containing 0.02% (w/v) Tween 20, the wells were blocked with 1% (w/v) bovine serum albumin (BSA) in PBS for 1 hr at 37° C. Mouse sera dilutions or undiluted hybridoma supernatants were incubated on coated plates for 1 hour at 37° C. Plates were washed and probed with HRP-labeled goat anti-murine IgG (Sigma) diluted 1:10,000 in 1% BSA/PBS for 30 minutes at 37° C. Plates were again washed then incubated for 15 minutes at RT with 100 μL/well of citrate-phosphate substrate solution (0.1 M citric acid and 0.2 M sodium phosphate, 0.01% H₂O₂, and 1 mg/mL OPD). Substrate development was stopped by addition of 4N sulfuric acid at 25 μL/well and the absorbance was measured at 490 nm via an automated plate spectrophotometer. Because the CNGH0010 protein generated in-house contains a His-tag, the reactive hybrids were cross-screened against His to determine specificity to CNGH0010. Plates were coated with hexa-his (Centocor) as described above and positive hybrid supernatants were incubated, probed and developed as described. All hybrid cell lines that demonstrated specificity to CNGH0010 were subcloned twice by limiting dilution at 1 cell/well in cloning plates. The homogeneous cell lines were cryopreserved in freezing medium (90% FBS, 10% DMSO) and stored in liquid nitrogen.

Binding characteristics for the antibodies were assessed using a solid phase CNGH0010 EIA. CNGH0010 coated plates were incubated with antibody supernatants with known IgG concentrations in two-fold serial dilutions from a starting concentration of 5 μg/mL for 30 minutes at 37° C. Plates were washed, probed and processed as described above.

Example 9 Mouse Anti-CNGH0010 Affinity Analysis

Mouse anti-CNGH0010 monoclonal antibodies were individually captured on anti-murine Fc surfaces of a Biacore 3000 biosensor. CNGH0010.2 was injected in duplicate at increasing concentrations (7.4 to 600 nM). Affinities were calculated from the ratio of measured rate constants (k_(d)/k_(a)) and are shown in Table 6.

TABLE 6 Kinetic analysis data mAb Capture (RU) k_(a) M⁻¹ s⁻¹ k_(d) s⁻¹ K_(D) nM 1291 300 6.24 × 10⁴ ± 0.01  5.1 × 10⁻⁴ ± 0.2 8.1 1292 400 7.09 × 10⁴ ± 0.02  1.0 × 10⁻⁵ <0.14 1324 200 2.66 × 10⁴ ± 0.01 1.25 × 10⁻³ ± 0.04 46.9 1329 290 8.21 × 10⁴ ± 0.02  9.5 × 10⁻⁴ ± 0.1 11.6 1332 325 1.35 × 10⁵ ± 0.04 2.21 × 10⁻³ ± 0.02 16.3 1333 200 1.41 × 10⁵ ± 0.01   4 × 10⁻⁴ 7.0 1339 200 5.00 × 10⁴ ± 0.02   7 × 10⁻⁵ ± 1 1.4 1354 230 6.55 × 10⁴ ± 0.02  1.0 × 10⁻⁵ <0.15

Example 10 CNGH0010 Expression Analysis in Tissues

Protocols for immunohistochemistry have been previously described (D'Andrea, et al, 1994; D'Andrea et al, 1998a). All incubations were performed at room temperature. After microwaving the slides in Target (Dako, Carpenturia, Calif.), the slides were placed in dH₂O, then 3% H₂O₂, rinsed in 10× Automation Buffer (Biomeda), treated with Avidin blocking, rinsed in buffer, & treated with Biotin blocking (15 minutes each, from Vector, catalog #SP-2001). Normal goat blocking serum (Vectastain, PK-6101) was then added for 10 minutes. Subsequently, the rabbit polyclonal primary antibody to 58 (or 60) (homemade antibodies) was applied to the slides for 30 minutes. Antibody diluent (Zymed, 00-3118) was substituted as the primary antibody for the negative control. After several PBS washes, a biotinylated secondary goat anti-rabbit antibody (Vector Labs, Burlingame, Calif.) was placed on the slides for 30 minutes. Subsequently, the slides were washed in PBS and then the avidin-biotin complex (ABC, Vector Labs, Burlingame, Calif.) was applied to the slides for 30 minutes. The presence of the primary antibodies was detected by adding DAB (3′-diaminobenzidine HCl; Biomeda, Foster City, Calif.) for 2 times 5 minutes each. Slides were briefly exposed to Mayer's hematoxylin (Sigma-Aldrich, MHS-32) for 1 minute, dehydrated and coverslipped.

Utilizing the rabbit polyclonal anti-CNGH0010 antibody to immunolocalize CNGH0010 isoforms in tissues and tumors, it is obvious that this gene product is expressed in a variety of both epithelial and non-epithelial tissues, including kidney, pancreas, lung, and skin. Specifically, CNGH0010 is expressed in the tubular epithelium of the kidney, the islet cells of the pancreas, the endothelial cells and macrophages of the lung, and the differentiated keratinocytes of the skin. Similarly, CNGH0010 is over-expressed in a number of tumors of both epithelial (carcinomas) and non-epithelial (sarcomas) origin, e.g., esophagus, gastro-intestinal stromal, liver, lung, osteosarcom, squamous cell (skin), thyroid, basal cell carcinoma, breast, and colon. It remains to be seen if the observed CNGH0010 over-expression in these tumors confers any growth advantage to them.

Example 11 In Situ Hybridization

Fragments from the CNGH0010 cDNA were cloned into pGEM3Z for in vitro transcription using digoxigenin labeled ribonucleotides. Sense and anti-sense riboprobes were generated from these vectors after linearization with appropriate restriction enzymes. Plasmid p3533 was used to generate a CNGH0010.1 and 10.2 specific riboprobe using the SP6 promoter (FIG. 8A), and plasmid p3534 was used to generate a CNGH0010.1 and 10.5 specific riboprobe using the T7 promoter (FIG. 8B).

Human skin and human multi-tissue slides were routinely dewaxed and left to air dry for 30 minutes at room temperature. The tissues were digested with pepsin (Invitrogen, Carlsbad, Calif.) for 10 minutes at 37° C. Following this digestion, slides were washed briefly in dH₂O and placed into 3% H₂O₂ for 10 minutes at room temperature. The slides were thoroughly washed, dehydrated in alcohols 70%-95% for 1 minute each and then left again to air dry for 30 minutes at room temperature. Each probe was diluted to 15.0 ng/μl (Table 1) in probe diluent (Biomeda, Foster City, Calif.). Fifty microliters of probe cocktail was added on the tissue and a cover slip was placed atop the solution. The slides were denatured for 10 minutes at 95° C. and then placed into a humidity chamber (Slide Moat, Boekel Scientific, Feasterville, Pa.) for a 37° C. overnight incubation. After hybridization, the slides were then immediately placed into a low stringency wash (2×SSC for 5 minutes at 42° C.) and then into a high stringency wash (0.1×SSC) for 5 minutes at 42° C. The slides were washed in 1× auto buffer and then incubated with a horseradish peroxidase anti-dig antibody (anti-digoxigenin-POD, Fab fragments, Roche, Indianapolis, Ind.) for 1 hour at room temperature. The slides were washed and then exposed to 3-3′ diaminobenzidine tetrahydrochloride chromogen for 2 times 5 minutes at room temperature. The slides were routinely stained with hematoxylin and then dehydrated, cleared in xylene, coverslipped in Permount (Fisher Scientific, Pittsburg, Pa.) then photographed under an Olympus BX51 light microscope. The positive control included a digoxigenin labeled mRNA riboprobe, β-actin. The negative controls included 1) the absence of the probe in the probe cocktail; 2) a sense strand of the targeted probed; and 3) pre-digestion of the tissues with a high concentration of RNase (32.5 mg/ml, Sigma, St. Louis, Mo.) for 2 hours at 37° C.

As shown in FIGS. 9A-F, in situ hybridization analysis of CNGH0010 shows expression in various tissues: breast (FIG. 9A), small intestine (FIG. 9B), skin (FIG. 9C), prostate (FIG. 9AD), liver (FIG. 9E), and pancreas (FIG. 9F). A digoxigenin labeled anti-sense riboprobe specific for the 5′ and 3′ ends of the CNGH0010 gene was used in the analysis. A sense probe was used to assess non-specific hybridization, and was negative on all samples (data not shown). The data obtained localizes the expression of the CNGH0010 gene to 6 epithelial tissue types that are often the sites of inflammation in various disease states. As a result, this data can allow the determination of which tissues to target for therapy with CNGH0010 agonists and/or antagonists, e.g., anti-CNGH0010 therapeutics. For example, CNGH0010 may be relevant to pathologic conditions like inflammatory disorders and cancer.

Although illustrated and described above with reference to certain specific embodiments, the present invention is nevertheless not intended to be limited to the details shown. Rather, the present invention is directed to the CNGH0010 polypeptides, polynucleotides, antibodies, apparatus, and kits disclosed herein and uses thereof, and various modifications may be made in the details within the scope and range of equivalents of the claims and without departing from the spirit of the invention. 

1. An isolated nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS:2, 4, 6, 8, 10, and 40 or an exact complement of said nucleotide sequence.
 2. An isolated nucleic acid molecule comprising a nucleotide sequence encoding a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NOS:3, 5, 7, 9, 11, and
 41. 3. An isolated nucleic acid molecule encoding a naturally occurring allelic variant of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NOS:3, 5, 7, 9, 11, and
 41. 4. An isolated nucleic acid molecule comprising a nucleotide sequence having at least 90% identity to any one of SEQ ID NOS:2, 4, 6, 8, 10, and 40 or an exact complement of said nucleotide sequence.
 5. An isolated nucleic acid molecule comprising a nucleotide sequence having at least 70% identity to any one of SEQ ID NOS :2, 4, 6, 8, 10, and 40 or an exact complement of said nucleotide sequence.
 6. An isolated nucleic acid molecule comprising a nucleotide sequence of at least 45 nucleotide residues having at least 90% identity to a portion of any one of SEQ ID NOS:2, 4, 6, 8, 10, and 40 or an exact complement of said nucleotide sequence.
 7. An isolated nucleic acid molecule encoding a fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NOS:3, 5, 7, 9, 11, and 41 wherein the fragment has an amino acid sequence comprising at least 15 consecutive amino acid residues of an amino acid sequence selected from the group consisting of SEQ ID NOS:3, 5, 7, 9, 11, and
 41. 8. The nucleic acid molecule of claim 1, wherein the nucleotide sequence further comprises a portion encoding a heterologous polypeptide.
 9. The nucleic acid molecule according to claim 1, further comprising vector nucleic acid residues.
 10. A vector comprising the nucleic acid molecule of claim 9
 11. A host cell containing the nucleic acid molecule of claim
 9. 12. The host cell of claim 11, wherein the host cell is of mammalian, bacterial, yeast, or insect origin.
 13. A kit comprising (i) a compound hybridizing with a nucleic acid molecule having a nucleotide sequence with at least 95% identity to any of SEQ ID NOS:1, 2, 4, 6, 8, and 10 in 6×SSC at about 45° C. followed by washing in 0.2×SSC, 0.1% SDS at about 65° C., and (ii) instructions for use.
 14. An isolated polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOS:3, 5, 7, 9, 11, and
 41. 15. An isolated polypeptide comprising a naturally occurring allelic variant of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NOS:3, 5, 7, 9, 11, and
 41. 16. An isolated polypeptide comprising an amino acid sequence having at least 90% identity to an amino acid sequence selected from the group consisting of SEQ ID NOS:3, 5, 7, 9, 11, and
 41. 17. An isolated polypeptide comprising at least 15 contiguous amino acids of an amino acid sequence selected from the group consisting of SEQ ID NOS:3, 5, 7, 9, 11, and
 41. 18. A fusion polypeptide comprising the polypeptide of claim 14 operably linked to a heterologous polypeptide.
 19. The fusion polypeptide of claim 18 wherein the heterologous polypeptide is a member of the immunoglobulin protein family or a fragment of said member.
 20. The polypeptide according to claim 14, wherein said polypeptide has at least one activity of a CNGH0010 polypeptide.
 21. The polypeptide of claim 20, wherein the polypeptide is glycosylated.
 22. The polypeptide of claim 21, wherein the polypeptide is O-linked glycosylated.
 23. An antibody comprising a monoclonal or polyclonal antibody, fusion protein, or fragment thereof, specifically binding to a polypeptide according to claim
 14. 24. An isolated nucleic acid molecule encoding the antibody of claim
 23. 25. A method for producing at least one CNGH0010 antibody, comprising translating the nucleic acid molecule of claim 24, under conditions in vitro, in vivo or in situ, wherein the CNGH0010 antibody is expressed in detectable or recoverable amounts.
 26. An antibody produced by the method of claim
 25. 27. A vector comprising the isolated nucleic acid molecule of claim
 24. 28. A host cell comprising the isolated nucleic acid molecule of claim 24, wherein the host cell is prokaryotic or eukaryotic.
 29. The host cell of claim 28, wherein the host cell is one or more selected from COS-1, COS-7, HEK293, BHK21, CRO, BSC-1, Hep G2, 653, SP2/0, 293, HeLa, myeloma, and lymphoma cells, or any derivative, immortalized or transformed cell thereof.
 30. A method for producing at least one CNGH0010 polypeptide, comprising translating the nucleic acid molecule of claim 1, under conditions in vitro, in vivo or in situ, wherein the CNGH0010 polypeptide is expressed in detectable or recoverable amounts.
 31. A polypeptide produced by the method of claim
 30. 32. A method for generating antibodies for a polypeptide, comprising immunizing or screening recombinant antibodies with a polypeptide according to claim
 14. 33. A composition comprising the nucleic acid molecule of claim 1, a polypeptide encoded by the nucleic acid, or an antibody to the polypeptide.
 34. A composition comprising an agonist or antagonist of one or more of the nucleic acid molecule of claim 1, a polypeptide encoded by the nucleic acid molecule, or an antibody to the polypeptide.
 35. The composition of claim 34, wherein said composition further comprises a pharmaceutically acceptable carrier or diluent.
 36. The composition of claim 34, administered in combination with a composition comprising one or more compound, composition or polypeptide selected from the group consisting of a detectable label or reporter, a TNF antagonist, an anti-infective drug, a cardiovascular (CV) system drug, a central nervous system (CNS) drug, an autonomic nervous system (ANS) drug, a respiratory tract drug, a gastrointestinal (GI) tract drug, a hormonal drug, a drug for fluid or electrolyte balance, a hematologic drug, an antineoplastic, an immunomodulation drug, an opthalmic, otic or nasal drug, a topical drug, a nutritional supplement, a cytokine, and a cytokine antagonist.
 37. The composition of claim 34, in a form of one or more selected from the group consisting of a liquid or gas solution, mixture, suspension, emulsion or colloid, a lyophilized preparation, and a powder.
 38. A method for diagnosing a CNGH0010-related condition in a cell, tissue, organ or animal, comprising contacting or administering a composition comprising means for detection of one or more of the nucleic acid molecule of claim 1, a polypeptide encoded by the nucleic acid molecule, or an antibody to the polypeptide, in said cell, tissue, organ or animal.
 39. A method for treating a CNGH0010-related condition in a cell, tissue, organ or animal, comprising contacting or administering to a patient a composition comprising an effective amount of one or more of the composition of claim 33 or an agonist or antagonist to the composition, with or to said cell, tissue, organ or animal.
 40. A method according to claim 39 wherein said effective amount is about 0.001-50 mg of the antibody; about 0.000001-500 mg of the polypeptide; or about 0.0001-100 μg of the nucleic acid molecule per kilogram of said cells, tissue, organ or animal.
 41. A method according to claim 39, wherein said contact or administration is by one or more modes selected from the group consisting of parenteral, subcutaneous, intramuscular, intravenous, intrarticular, intrabronchial, intraabdominal, intracapsular, intracartilaginous, intracavitary, intracelial, intracerebellar, intracerebroventricular, intracolic, intracervical, intragastric, intrahepatic, intramyocardial, intraosteal, intrapelvic, intrapericardiac, intraperitoneal, intrapleural, intraprostatic, intrapulmonary, intrarectal, intrarenal, intraretinal, intraspinal, intrasynovial, intrathoracic, intrauterine, intravesical, intralesional, bolus, vaginal, rectal, buccal, sublingual, intranasal, and transdermal.
 42. A method according to claim 41, further comprising administering, prior, concurrently or after said contacting or administering step, at least one composition comprising an effective amount of one or more compound or polypeptide selected from the group consisting of a detectable label or reporter, a TNF antagonist, an anti-infective drug, a cardiovascular (CV) system drug, a central nervous system (CNS) drug, an autonomic nervous system (ANS) drug, a respiratory tract drug, a gastrointestinal (GI) tract drug, a hormonal drug, a drug for fluid or electrolyte balance, a hematologic drug, an antineoplastic, an immunomodulation drug, an opthalmic, otic or nasal drug, a topical drug, a nutritional supplement, a cytokine, and a cytokine antagonist.
 43. A method for treating a CNGH0010-related condition in a cell, tissue, organ or animal, comprising contacting or administering to a patient a composition comprising an effective amount of one or more modulator of CNGH0010 nucleic acid molecule or CNGH0010 polypeptide levels or a modulator of CNGH0010 activity in said cell, tissue, organ or animal.
 44. A method for treating an epithelial-related condition in a cell, tissue, organ or animal, comprising contacting or administering to a patient a composition comprising an effective amount of the composition of claim 33 or an agonist or antagonist to the composition, with or to said cell, tissue, organ or animal.
 45. A method for treating an epithelial-related condition in a cell, tissue, organ or animal, comprising contacting or administering to a patient a composition comprising an effective amount of at least one modulator of CNGH0010 nucleic acid molecule or CNGH0010 polypeptide levels or a modulator of CNGH0010 activity in said cell, tissue, organ or animal.
 46. A device comprising one or more of the nucleic acid molecule of claim 1, a polypeptide encoded by the nucleic acid molecule, and an antibody, agonist or antagonist to the polypeptide, wherein said device is suitable for contacting or administering one or more of said polypeptide, antibody, agonist, antagonist, or nucleic acid molecule, by one or more modes selected from the group consisting of parenteral, subcutaneous, intramuscular, intravenous, intrarticular, intrabronchial, intraabdominal, intracapsular, intracartilaginous, intracavitary, intracelial, intracerebellar, intracerebroventricular, intracolic, intracervical, intragastric, intrahepatic, intramyocardial, intraosteal, intrapelvic, intrapericardiac, intraperitoneal, intrapleural, intraprostatic, intrapulmonary, intrarectal, intrarenal, intraretinal, intraspinal, intrasynovial, intrathoracic, intrauterine, intravesical, intralesional, bolus, vaginal, rectal, buccal, sublingual, intranasal, and transdermal.
 47. An article of manufacture for human pharmaceutical or diagnostic use, comprising packaging material and a container comprising one or more of the nucleic acid molecule of claim 1, a polypeptide encoded by the nucleic acid molecule, and an antibody, agonist or antagonist to the polypeptide.
 48. The article of manufacture of claim 47, wherein said container is a component of a parenteral, subcutaneous, intramuscular, intravenous, intrarticular, intrabronchial, intraabdominal, intracapsular, intracartilaginous, intracavitary, intracelial, intracerebellar, intracerebroventricular, intracolic, intracervical, intragastric, intrahepatic, intramyocardial, intraosteal, intrapelvic, intrapericardiac, intraperitoneal, intrapleural, intraprostatic, intrapulmonary, intrarectal, intrarenal, intraretinal, intraspinal, intrasynovial, intrathoracic, intrauterine, intravesical, intralesional, bolus, vaginal, rectal, buccal, sublingual, intranasal, or transdermal delivery device or system.
 49. A method for producing one or more of the nucleic acid molecule of claim 1, a polypeptide encoded by the nucleic acid molecule, and an antibody, agonist or antagonist to the polypeptide, comprising providing one or more vector, host cell, transgenic animal, transgenic plant, or plant cell capable of transcribing said nucleic acid and/or expressing in detectable or recoverable amounts said polypeptide or antibody.
 50. A polypeptide, antibody, agonist, antagonist or nucleic acid molecule, produced by the method of claim
 49. 51. A method for detecting the presence or absence of the nucleic acid molecule according to claim 1 or a polypeptide encoded by the nucleic acid molecule in a biological sample, comprising obtaining a biological sample from a test subject and contacting the biological sample with a compound or an agent capable of detecting said polypeptide wherein the presence of the polypeptide or nucleic acid molecule is detected in the biological sample.
 52. An isolated nucleic acid molecule comprising a nucleotide sequence of nucleotides 10 1-526 (Exon 1), 786-986 (Exon 2), 1099-1155 (Exon 3), 1763-1813 (Exon 4), 1983-2165 (Exon 5), 3324-3392 (Exon 8), 7590-7637 (Exon 13), 7811-7858 (Exon 14), 10690-10746 (Exon 16), 11393-11440 (Exon 17), 12996-13043 (Exon 19), 13547-13618 (Exon 21), 14679-14702 (Exon 22), 14813-14860 (Exon 23), and 16038-16356 (Exon 25) of SEQ ID NO:1 and, optionally, one or more from the group consisting of nucleotides 2936-2980 (Exon 6), 3615-3665 (Exon 9), 5336-5371 (Exon 10), 6065-6118 (Exon 11), 7391-7450 (Exon 12), 13157-13198 (Exon20), and 15895-15929 (Exon24) of SEQ ID NO:1, or an exact complement of said nucleotide sequence.
 53. An isolated nucleic acid molecule comprising a nucleotide sequence of nucleotides 10 1-526 (Exon 1), 786-986 (Exon 2), 1099-1155 (Exon 3), 1763-1813 (Exon 4), 1983-2165 (Exon 5), 3324-3392 (Exon 8), 7590-7637 (Exon 13), 7811-7858 (Exon 14), and 10129-10155 (Exon 15) of SEQ ID NO:1 and, optionally, one or more from the group consisting of nucleotides 3615-3665 (Exon 9), 5336-5371 (Exon 10), 6065-6118 (Exon 11), and 7391-7450 (Exon 12) of SEQ ID NO:1, or an exact complement of said nucleotide sequence.
 54. An isolated nucleic acid molecule comprising a nucleotide sequence of nucleotides 3149-3205 (Exon 7), 3324-3392 (Exon 8), 7590-7637 (Exon 13), 7811-7858 (Exon 14), 10690-10746 (Exon 16), 11393-11440 (Exon 17), 12996-13043 (Exon 19), 13547-13618 (Exon21), 14679-14702 (Exon 22), 14813-14860 (Exon 23), and 16038-16356 (Exon 25) of SEQ ID NO: 1 and, optionally, one or more from the group consisting of nucleotides 3615-3665 (Exon 9), 5336-5371 (Exon 10), 6065-6118 (Exon 11), 7391-7450 (Exon 12), 13157-13198 (Exon20), and 15895-15929 (Exon24) of SEQ ID NO:1, or an exact complement of said nucleotide sequence.
 55. An isolated nucleic acid molecule comprising a nucleotide sequence of nucleotides 3149-3205 (Exon 7), 3324-3392 (Exon 8), 7590-7637 (Exon 13), 7811-7858 (Exon 14), and 10129-10155 (Exon 15) of SEQ ID NO: 1 and, optionally, one or more from the group consisting of nucleotides 3615-3665 (Exon9), 5336-5371 (Exon 10), 6065-6118 (Exon 11), and 7391-7450 (Exon 12) of SEQ ID NO:1, or an exact complement of said nucleotide sequence.
 56. An isolated nucleic acid molecule comprising a nucleotide sequence of nucleotides 101-526 (Exon 1), 786-986 (Exon 2), 1099-1155 (Exon 3), 1763-1813 (Exon 4), 1983-2165 (Exon 5), 3324-3392 (Exon 8), 7391-7450 (Exon 12), and 7590-7637 (Exon 13) of SEQ ID NO:1, or an exact complement of said nucleotide sequence.
 57. An isolated nucleic acid molecule comprising a nucleotide sequence having at least 90% identity to any of the nucleotide sequences recited in claim 52, or an exact complement of said nucleotide sequence.
 58. An isolated nucleic acid molecule encoding a fragment of a polypeptide having an amino acid sequence encoded by any of the nucleotide sequences recited in claim 52, wherein the fragment has an amino acid sequence comprising at least 15 consecutive amino acid residues of an amino acid sequence encoded by any of the nucleotide sequences recited in claim
 52. 59. The nucleic acid molecule according to claims 52, wherein the nucleotide sequence further comprises a portion encoding a heterologous polypeptide.
 60. The nucleic acid molecule according to any of claim 52, further comprising vector nucleic acid residues.
 61. A vector comprising the nucleic acid molecule of claim
 60. 62. A host cell containing the nucleic acid molecule of claim
 60. 63. The host cell of claim 62, wherein the host cell is of mammalian, bacterial, yeast, or insect origin.
 64. A kit comprising (i) a compound hybridizing with a nucleic acid molecule having a nucleotide sequence with at least 95% identity to the nucleotide sequences according to claim 52 in 6×SSC at about 45° C. followed by washing in 0.2×SSC, 0.1% SDS at about 65° C., and (ii) instructions for use.
 65. An isolated polypeptide encoded by any of the nucleotide sequences according to claim
 52. 66. An isolated polypeptide comprising an amino acid sequence having at least 90% identity to the amino acid sequence encoded by any of the nucleotide sequences according to claim
 52. 67. An isolated polypeptide comprising at least 15 contiguous amino acids of the amino acid sequence encoded by any of the nucleotide sequences according to claim
 52. 68. A fusion polypeptide comprising the polypeptide of claim 65 operably linked to a heterologous polypeptide.
 69. The fusion polypeptide of claim 68 wherein the heterologous polypeptide is a member of the immunoglobulin protein family or a fragment of said member.
 70. The polypeptide according to claim 65, wherein said polypeptide has at least one activity of a CNGH0010 polypeptide.
 71. An antibody comprising a monoclonal or polyclonal antibody, fusion protein, or fragment thereof, specifically binding to the polypeptide of claim
 65. 72. An isolated nucleic acid molecule encoding the antibody of claim
 71. 73. A method for producing an antibody, comprising translating the nucleic acid molecule of claim 72, under conditions in vitro, in vivo or in situ, wherein the antibody is expressed in detectable or recoverable amounts.
 74. An antibody produced by the method of claim
 73. 75. A vector comprising the isolated nucleic acid molecule of claim
 72. 76. A host cell comprising the isolated nucleic acid molecule of claim 72, wherein the host cell is prokaryotic or eukaryotic.
 77. The host cell of claim 76, wherein the host cell is one or more selected from COS-1, COS-7, HEK293, BHK21, CRO, BSC-1, Hep G2, 653, SP2/0, 293, HeLa, myeloma, and lymphoma cells, or any derivative, immortalized or transformed cell thereof.
 78. A method for producing a CNGH0010 polypeptide, comprising translating the nucleic acid molecule according to claim 52, under conditions in vitro, in vivo or in situ, wherein the CNGH0010 polypeptide is expressed in detectable or recoverable amounts.
 79. A polypeptide produced by the method of claim
 78. 80. A method for generating antibodies for a polypeptide, comprising immunizing or screening recombinant antibodies with a polypeptide according to claim
 65. 81. A composition comprising one or more of the nucleic acid molecule according to claim 52, a polypeptide encoded by the nucleic acid molecule, and an antibody to the polypeptide.
 82. A composition comprising an agonist or antagonist of one or more of the nucleic acid molecule according to claim 52, a polypeptide encoded by the nucleic acid molecule, and an antibody to the polypeptide.
 83. The composition of claim 82, wherein said composition further comprises at least one pharmaceutically acceptable carrier or diluent.
 84. An isolated nucleic acid molecule comprising a truncated CNGH0010 nucleotide sequence containing one or more from the group consisting of nucleotides 1983-2076 (Exon 5a), 2117-2165 (Exon 5b), 3168-3197 (Exon 7a), and 3189-3393 (Exon 8a) of SEQ ID NO:1.
 85. Any invention described herein. 